Vaccines against toxoplasma gondii

ABSTRACT

Vaccines are disclosed against parasites. The vaccines include peptides in an immunological composition. In particular, the parasite is  Toxoplas gondii.

This application is a U.S. nationalization under 35 U.S.C. §371 of International Application No. PCT/US2011/059147, filed Nov. 3, 2011, which claims priority to Provisional Application No. 61/456,309, filed Nov. 4, 2010. The disclosures set forth in the referenced applications are incorporated herein by reference in their entireties.

This invention was made with Government support under Grant Number NIH U01 AI77887. The government has certain rights to this invention.

SEQUENCE LISTING

The instant application contains a Sequence Listing which has been submitted in ASCII format via EFS-Web and is hereby incorporated by reference in its entirety. Said ASCII copy, created on Dec. 30, 2011, is named 21459921.txt and is 12,384 bytes in size.

BACKGROUND

Toxoplasmosis refers to a disease caused by the parasite Toxoplasma gondii (T. gondii). The active infection destroys tissues, especially brain and eye in the fetus, newborn infant, immune compromised persons and those with retinal disease. In the presence of a normal immune response, the parasite remains as a chronic cryptic, latent brain infection, that can recrudesce and thus cause eye damage throughout the life of the host. About four thousand cases of newly active retinal disease are diagnosed in the U.S. each year. Importantly, this parasite chronically infects 30-50% of human population worldwide, with unknown consequences of this chronic infection of the brain in 2-3 billion persons throughout the world. Herein we describe various embodiments of an immunosense vaccine consisting of peptides created from immunogenic parasite proteins.

Human cells have a major histocompatibility complex (MHC) Class I processing pathway in which the proteasome in the cytosol degrades proteins from T. gondii into chains of eight to ten amino acids. These peptides associated with MHC Class I molecules then travel through the endoplasmic reticulum, and are presented at the surface of all cells so that the T cell receptors of cytotoxic T cells (CTLs) and IFN-γ producing CD8⁺ T cells can recognize the MHC molecule and bound peptide. Thus, IFN-γ producing CD8⁺ T cells are able to identify the peptides as self or non-self. Cells that present non-self peptides are killed and/or elicit IFN-γ. In this manner, CD8⁺ T lymphocytes play a major role in protection against T. gondii by secreting IFN-γ which activates macrophages to inhibit replication, kill the parasite, and induce lysis of infected cells. Thus, this obligate intracellular parasite loses its intracellular niche.

Since CD8⁺ T cells recognize target cells by peptide epitopes presented in the context of MHC Class I molecules, it is of great interest to identify MHC Class I restricted peptide epitopes from specific T. gondii antigens to facilitate creating vaccines that stimulate cell-mediated immune responses. The identification of CD8⁺ T cell responses provides peptide antigens that can be used for directly monitoring CD8⁺ T cell responses resulting from vaccination.

Toxoplasma gondii is an intracellular parasite which infects a broad range of mammalian hosts and can cause severe disease in immune-compromised or immunologically immature persons. The infection can cause severe ocular, neurologic, and systemic disease in these settings. Because no medicines eradicate all life cycle stages of this parasite, development of a vaccine against T. gondii is extremely useful, especially a vaccine that can prevent acquisition of parasite completely.

A preferred vaccine to protect against toxoplasmosis in humans includes epitopes that elicit a protective Th1 biased-immune response, characterized by the generation of long-lived IFN-γ-producing CD8⁺ T cells. CD4⁺ and CD8⁺ T cells have a critical role in protective immunity to T. gondii in murine models and humans. CD8⁺ T cells and interferon gamma (IFN-γ) are significant effectors mediating resistance to acute and chronic T. gondii infection. Peptide-based vaccines derived from CD8⁺ T cell epitopes are a promising strategy to mobilize the immune system against T. gondii in humans. However, until now no T. gondii specific HLA restricted CD8⁺ T cell epitopes that were proven to be protective had been identified.

SUMMARY

I. An Immunosense Vaccine to Prevent Toxoplasmosis: Protective Toxoplasma gondii Epitopes Restricted by HLA-A*0201

A vaccine to protect against toxoplasmosis in humans preferably includes antigens that elicit a protective T helper cell type 1 immune response, and generates long-lived IFN-γ-producing CD8⁺ T cells. Herein, a predictive algorithm was utilized to identify candidate HLA-A02 supertype epitopes from T. gondii proteins. Thirteen peptides elicited production of IFN-γ from PBMC of HLA-A02 supertype persons seropositive for T. gondii infection, but not from seronegative controls. These peptides displayed high-affinity binding to HLA-A02 proteins. Immunization of HLA-A*0201 transgenic mice with these pooled peptides, with a universal CD4⁺ epitope peptide called PADRE, formulated with adjuvant GLA-SE, induced CD8⁺ T cell IFN-γ production and protected against parasite challenge. Peptides identified are useful in immunosense epitope-based vaccines.

HLA-A02 restricted epitopes from T. gondii have been identified. These epitopes have been evaluated as components in a candidate vaccine by immunizing HLA-A*0201 transgenic mice to determine whether they could provide protection against T. gondii challenge. The effect of adjuvants in poly-epitope immunizations has been evaluated for this supermotif immunosense vaccine. Accordingly, GRA10, GRA15, SAG2C, SAG2D, SAG2X, SAG3, SRS9, BSR4, SPA, and MIC proteins from T. gondii were screened for CD8⁺ T cell epitopes by using an HLA motif algorithm in the immunoepitope database (IEDB). This was intended to predict potential epitopes that would bind to the HLA-A02 supertype family, which is present in 50% of the population worldwide, irrespective of ethnicity. Ten nonamer T. gondii derived peptides derived from the amino acid sequence of SAG2C₃₈₋₄₆, SAG2D₁₈₀₋₁₈₉, SAG2X₄₄₋₅₂, SAG²X₃₅₁₋₃₅₉, SAG3₁₃₆₋₁₄₄, SAG3₃₇₅₋₃₈₃, SPA₁₂₋₂₀, SPA₈₂₋₉₀, MIC1₉₋₁₇, and MICA2P₁₁₋₁₉ were identified via bioinformatic and affinity binding assays and tested in ELISpot assays with peripheral blood mononuclear cells from HLA-A*0201 T. gondii-seropositive individuals. SAG1, SUSA1, GRA2, GRA3, GRA6, GRA7, ROP2, ROP16, and ROP18 were also screened and GRA6₂₄₋₃₂ (VVFVVFMGV (SEQ ID NO: 1)), GRA6₂₉₋₃₇ (FMGVLVNSL (SEQ ID NO: 2)), and GRA3₂₅₋₃₃ (FLVPFVVFL (SEQ ID NO: 3)) also had been found to elicit IFN-γ from PBMC from seropositive but not seronegative persons (Tan T G et al., 2010). HLA-A*0201 transgenic mice immunized with the newly identified peptides, and the three HLA-A02 peptides identified previously were all pooled. They were administered with the CD4⁺ helper T cell peptide PADRE and the adjuvant, GLA-SE, which induced high levels of IFN-γ production and protected mice against challenge from type II parasites.

II. Immunosense Based Vaccine Protects HLA-A*1101 Transgenic Mice Against Toxoplasmosis

In another embodiment, a humanized HLA-A*1101 (an HLA-A03 supertype haplotype) transgenic mouse model was used to create/assess protective efficacy of a human CD8⁺ T cell epitope-based vaccine against primary Toxoplasma gondii infection. Peptide-based approaches to induce IFN-γ responses were evaluated to provide a foundation for development of immunosense vaccines for human use. Three immunodominant human CD8⁺ T-cell peptide epitopes, KSFKDILPK (SAG ¹ ₂₂₄₋₂₃₂) (SEQ ID NO: 4); AMLTAFFLR (GRA6₁₆₄₋₁₇₂) (SEQ ID NO: 5); RSFKDLLKK (GRA⁷ ₁₃₄₋₁₄₂) (SEQ ID NO: 6), were joined with a universal human CD4⁺ T cell peptide epitope PADRE (AKFVAAWTLKAAA (SEQ ID NO: 7)) to construct three separate pairs of CD4-CD8 lipopeptides or longer lipopeptides that linked the three peptides together. HLA-A*1101 transgenic mice were immunized with lipopeptides or a mixture of the peptides plus adjuvants, and T cell responses induced and protective efficacy were determined. Bioinformatic algorithms and binding studies identified additional CD8⁺ T cell peptides that elicited IFN-γ production by CD8⁺ T lymphocytes from HLA-A03 supertype donors. These peptides enhanced protection of HLA-A-1101 mice.

Peptide-based vaccines derived from CD8⁺ T cell epitopes are a promising strategy to mobilize the immune system against T. gondii in humans.

Three peptide epitopes from KSFKDILPK (SAG1₂₂₄₋₂₃₂) (SEQ ID NO: 4); AMLTAFFLR (GRA6₁₆₄₋₁₇₂) (SEQ ID NO: 5); and RSFKDLLKK (GRA7₁₃₄₋₁₄₂) (SEQ ID NO: 6) were identified to elicit IFN-γ from PBMCs of T. gondii from seropositive HLA-A03 supertype humans but not from PBMCs of T. gondii seronegative HLA-A03 supertype humans. (Tan, T. G., et al, 2010). Herein, 4 CD8⁺ T cell epitope containing vaccine formulations comprising lipopeptides that incorporate PADRE as well as an oil-in-water emulsion that includes a synthetic MLA derivative are described. The efficacy of various vaccine formulations consisting of the three CD8⁺ T cell peptides eliciting HLA-A*1101-restricted, CD8⁺ T cell-mediated IFN-γ production in vitro from HLA-A*1101 mice was examined.

Then, in order to identify additional peptides from T. gondii that are effective in eliciting IFN-γ from HLA-A03 supertype restricted CD8⁺ T cells, bioinformatic algorithms were utilized to identify additional, novel T. gondii-derived, CD8⁺ T cell epitopes restricted by the HLA-A03 supertype. The peptides from tachyzoite, bradyzoite and sporozoite proteins (GRA10, GRA15, SAG2C, SAG2D, SAG2X, SAG3, SRS9, BSR4, SPA, MIC) of the type II T. gondii strain, ME49, were screened searching for those with high binding scores in a bioinformatic analysis (IC₅₀<50 nM) and in binding assays. In addition, peripheral blood mononuclear cells from seropositive and seronegative persons were tested for response to these peptides using an IFN-γ ELISpot assay. These latter studies were used to identify other peptides for inclusion in a multi-epitope, next generation immunosense vaccine.

III. Immunization with a Toxoplasma gondii HLA-B*0702 Restricted GRA7₂₀₋₂₈ Peptide Plus Adjuvants Elicits IFN-γ from Human and Murine CD8⁺ T Cells and Protects HLA-B*0702 Mice Against Subsequent Parasite Challenge

CD8⁺ T cells have been shown to act as cytolytic effectors and produce IFN-γ to mediate resistance to Toxoplasma gondii in murine models due to recognition of peptides restricted by murine MHC Class I molecules. However, no T. gondii specific HLA-B07 restricted peptides were proven protective against T. gondii. Recently, two T. gondii-specific HLA-B*0702-restricted T cell epitopes, GRA7₂₀₋₂₈ (LPQFATAAT (SEQ ID NO: 8)) and GRA3₂₇₋₃₅ (VPFVVFLVA (SEQ ID NO: 9)), displayed high-affinity binding to HLA-B*0702, and elicited IFN-γ from PBMCs of seropositive HLA-B*0702 persons. Herein, these peptides were evaluated to determine whether they could immunize and protect HLA-B*0702 transgenic mice when administered with adjuvants. Peptide-specific IFN-γ producing T cells were identified by ELISPOT and proliferation assays utilizing splenic T lymphocytes from HLA transgenic mice. When HLA-B*0702 mice were immunized with one of the epitopes identified, GRA7₂₀₋₂₈ in conjunction with a universal CD4⁺ T cell epitope (PADRE) and adjuvants (CD4⁺ T cell adjuvant, MLA, and TLR2 stimulatory Pam₂Cys for CD8⁺ T cells), this immunization induced CD8⁺ T cells to produce IFN-γ and protected mice against high parasite burden when challenged with T. gondii. This work demonstrates feasibility of immunosense approaches for identifying protective HLA-B*0702 restricted T. gondii peptides and adjuvants that elicit protective immune responses in HLA-B*0702 mice.

Herein, these peptides identified earlier using bioinformatics and in vitro analyses were evaluated as vaccine components administered in conjunction with pan DR epitope (PADRE), a universal helper T lymphocyte epitope in HLA-B*0702 transgenic mice. Immunization of HLA-B*0702 transgenic mice with the peptide LPQFATAAT (SEQ ID NO: 8) with the help of PADRE and MLA and Pam₂Cys as adjuvants activated CD8⁺ T cells to produce IFN-γ and protected against subsequent challenge with a high burden of a type II parasite.

Previously, HF10 (HPGSVNEFDF (SEQ ID NO: 10)), a single decapeptide, derived from the dense granule protein 6 (GRA6) was identified as the protective, immunodominant L^(d)-restricted epitope in H-2^(d) mice infected with type II T. gondii parasite. This earlier work had reported that L^(d) was essential for restriction of cyst number and brain pathology in L^(d) mice. This also demonstrated that immunization of H-2L^(d) mice with the lipopeptide constructed by HF10 and PADRE or HF10 with monophosphoryl lipid A (MLA) protected Balb/c mice. However, HF10 administered to HLA-B07 transgenic mice in a similar manner was not immunogenic despite a common L^(d) and B7 peptide binding motif. Therefore, in order to find effective peptides for T. gondii derived HLA-B07⁺ restricted CD8⁺ T cells, bioinformatic algorithms were used to identify novel, T. gondii-derived, CD8⁺ T cell epitopes restricted by the HLA-B07 supertypes, which collectively provide coverage for 30% of the human population worldwide. The amino acid sequences from nine surface and secreted proteins (SAG1, SUSA1, GRA2, GRA3, GRA6, GRA7, ROP2, ROP16, ROP18) of the type II T. gondii strain, ME49, for HLA-B*0702-specific peptide binding scores were screened using bioinformatic analysis. Peripheral blood mononuclear cells from seropositive and seronegative persons were tested for response to these peptides using IFN-γ Elispot assay. Strikingly, two T. gondii-specific HLA-B*0702-restricted T cell epitopes, one derived from GRA7₂₀₋₂₈ (LPQFATAAT (SEQ ID NO: 8)), the other derived from GRA3₂₇₋₃₅ (VPFVVFLVA (SEQ ID NO: 9)) both displayed high-affinity binding to HLA-B*0702 and stimulated IFN-γ production by peripheral blood cells from HLA-B*0702 persons infected with T. gondii, but not seronegative controls.

BRIEF DESCRIPTION OF DRAWINGS

FIG. 1. IFN-γ ELISpot assay with pools of peptides that are predicted to bind avidly to HLA A02. (A) Twenty-nine HLA-A*02-restricted peptides were divided in 5 pools with 8 to 9 peptides per pool and tested for reactivity in PBMCs isolated from HLA-matched T. gondii-seropositive individuals in an ex vivo ELISpot assay. A2P1 to A2P5: peptide pools as described in Table 1. IFN-γ ELISpot assay with individual peptides in pool 1 and pool 2. DMSO, A2P2 (p<0.05); TLA, A2P1, A2P5 (p>0.05); A2P3 (P<0.01); A2P4 (p<0.001) (B) pool 3 and pool 4. FLSLSLLVI (SEQ ID NO: 11), FMIAFISCFA (SEQ ID NO: 12), FMIVSISLV (SEQ ID NO: 13) (P<0.05). (C) pool 5. FLTDYIPGA (SEQ ID NO: 14) (p<0.05); FLLGLLVHV (SEQ ID NO: 15) (p<0.01); FVIFACNFV (SEQ ID NO: 16), ITMGSLFFV (SEQ ID NO: 17), GLAAAVVAV (SEQ ID NO: 18) (p<0.001). (D) that bind to HLA supertype HLA-A02 This graph shows the spot count of each peptide tested for reactivity in PBMCs isolated from HLA-A02 T. gondii-seropositive individuals. The peptides are listed by their sequence and antigen. FAAAFFPAV (SEQ ID NO: 19) (p<0.05); VLLPVLFGV (SEQ ID NO: 20) (p<0.01). *, P<0.05; **P<0.01; ***P<0.001. FIG. 1B discloses SEQ ID NOS 55-60, 12, 11, 61, 12-13, and 62, respectively, in order of appearance. FIG. 1C discloses SEQ ID NOS 16, 63, 15, 14, 64-66, 17, 67-69, and 18, respectively, in order of appearance. FIG. 1D discloses SEQ ID NOS 20, 19, and 70-72, respectively, in order of appearance.

FIG. 2A. Schematic representation of the synthetic lipopeptide immunogens used. The C-terminal end of a promiscuous CD4⁺ T cell peptide epitope (PADRE) was joined in sequence with the N-terminal end of one of three differentT gondii CD8 T cell epitopes: SAG1₂₂₄₋₂₃₂ (A), GRA6₁₆₄₋₁₇₂ (B); GRA7₁₃₄₋₁₄₂ (C) or three epitopes linked together (D) with a three alanine linker. The N-terminal end of each resulting CD4-CD8 peptide was extended by a lysine covalently linked to one molecule of palmitic acid. This results in a four lipopeptides construct.

The abbreviation Lp is used herein to refer to the lipopeptide. When there is a mixture of components or undivided components they are named individually. Sequence of PADRE is AKFVAAWTLKAAA (SEQ ID NO: 7). Structure of Pam₂Cys is PAM₂KSS. FIG. 2A discloses the “Peptide Sequence in Lipopeptide” sequences as SEQ ID NOS 4-6 and 4-6, respectively, in order of appearance and the “Lipopeptide HLA A03 Supertype Vaccine Constructs” as SEQ ID NOS 73-76, respectively, in order of appearance.

FIG. 2B. HLA-A*1101 mice immunized with lipopeptides. Mice were immunized with lipopeptides: LpKS9, LpAM9, LpRS9 and LpKS9/AM9/RS9. The mice were immunized twice at three week intervals. Ten to fourteen days after the last immunization, spleen cells were separated from immunized mice and stimulated by appropriate peptides in an ex vivo IFN-γ ELISpot assay. Data presented are averages of three independent replicate experiments. *, P<0.05; **, P<0.01.

FIG. 3. HLA-A*1101 transgenic mice were immunized with peptide pool and adjuvants. Mice were immunized with (A) PBS, (B) peptide pool, (C) peptide pool with PADRE, (D) peptide pool with PADRE in GLA-SE, (E) peptide pool with PADRE and Pam2Cys in GLA-SE. Splenic T cells were isolated 10-14 days post-immunization and exposed to each peptide in an ex vivo IFN-g ELISpot assay.

FIG. 4. Immunogenicity of LT9 and VP9 in HLA transgenic mice. (A) HLA-B*0702-transgenic mice immunized with PBS as a control, peptides (LT9: LPQFATAAT (SEQ ID NO: 8); VA9: VPFVVFLVA (SEQ ID NO: 9)) prepared as follows: peptide alone, peptide plus PADRE, peptide plus PADRE and Pam₂Cys, all these immunogens mixed with MLA. Immunization was given three times at two week intervals. Ten to fourteen days after the last immunization, spleen cells were obtained from immunized mice and stimulated by the specified peptide in an ex vivo IFN-γ ELISPOT assay. (B) HLA-B*0702 mice immunized with peptide pools and tested for recall responses with LT9 or VA9 or PADRE. HLA-B*0702 transgenic mice immunized with mixtures of two identified peptides (LT9 and VA9), PADRE or Pam₂Cys mixed with MLA, three times at two week intervals. Fourteen days after the last immunization, spleens were removed from immunized mice and splenocytes were cultured with peptides, LT9 or VA9 or PADRE. The results are expressed as IFN-γ spot formation by one million cells. Data presented are a representative example from three independent experiments. (C) IFN-γ spot formation was significantly reduced in the presence of anti-CD8 antibody. Splenocytes from immunized mice were incubated with antibodies to CD8, and their isotype control for 60-90 min prior to stimulation with LT9 or VA9. *, P<0.05; **, P<0.01. IFN-γ spot formation was tested for splenocytes from mice that received different vaccine formulations in the absence or presence of blocking antibody.

FIG. 5. LT9-specific response induced by LT9 immunization. Mice were immunized with LT9 peptide alone, LT9/PADRE, LT9/PADREMLA/Pam₂Cys. IFN-γ production (A) and lymphocyte proliferation (B) were tested 2 weeks after last immunization. *, P<0.05; **, P<0.01

FIG. 6. PADRE-specific T cell responses were evaluated in immunized group. (A,B) PADRE-specific IFN-γ spot formation and spleen cell proliferation were tested by splenocytes from LT9 formulation immunized B7 mice exposed to PADRE peptide. *, P<0.05; **, P<0.01. (C) Blocking CD4⁺ T cell receptor using anti-CD4⁺ Ab significant decreases IFN-γ production in the following group.

FIG. 7. LT9 peptides with adjuvants induce HLA-B07-restricted CD8⁺ T cell responses in immunized mice. LT9-specific IFN-γ response and lymphocyte proliferation were measured by blocking CD8 (A,B) and HLA-B07®. In each immunization, the control is the left-hand bar. Splenocytes were isolated from peptide-immunized HLA-B07 transgenic mice 10 days after immunization and incubated with antibodies to CD8α or HLA-B07 and their common isotype control for 60-90 min prior to stimulation with LT9. Their abilities to generate IFN-γ and lymphocyte proliferation in response to peptide were tested. *, P<0.05; **, P<0.01.

FIG. 8. Replication of T. gondii luciferase expressing parasites were significant reduced in HLA-B07 mice immunized with LT9/PADRE/MLA/Pam₂Cys assayed from 6 days after challenge and cyst formation in day 30. HLA-B07 transgenic mice were either not immunized or immunized with LT9/PADRE/MLA/Pam₂Cys three times 14 days apart. Two weeks after vaccine administration, transgenic mice were challenged with 10,000 Pro(Fluc)-type II T. gondii luciferase expressing parasites. Average cyst enumeration was performed in the brains of mice challenged 30 days after final immunization. The data represent the means. There were a total of 5-9 mice tested in each control or immunization group. Asterisks indicate significant differences compared to the control.

DETAILED DESCRIPTION OF THE DISCLOSURE

I. Identification of HLA-A*0201-Restricted CD8⁺ T Cell Epitopes that Elicit IFN-γ from Seropositive Persons.

To identify candidate epitopes from Toxoplasma gondii that elicit IFN-γ from CD8⁺ T cells, the peptides derived from GRA10, GRA15, SAG2C, SAG2D, SAG2X, SAG3, SRS9, BSR4, SPA, and MIC were screened for potential supertype epitopes using the ARB, SMM, and ANN algorithms from immunoepitope database (IEDB) on the basis of their predicted binding affinity to HLA-A02 molecules. A total of 29 unique peptides IC₅₀<50 nM of all ranked nonameric or decameric peptides were selected (Cong, et al., (2011).

To determine which of these peptides would be recognized in the context of a Toxoplasma infection, peripheral blood mononuclear cells from T. gondii-seropositive HLA-A*0201 individuals were tested for response to these peptides in pools or individually by using an IFN-γ ELISpot assay. Candidate peptides were considered immunogenic if they induced IFN-γ spot formation that was significant compared to an irrelevant HLA-A*0201-restricted peptide. As shown in FIG. 1A, there were three peptide pools which stimulated significant response by human peripheral blood mononuclear cells (PBMC) derived from HLA-A02 seropositive individuals. Then the ability of individual peptides in each of these peptide pools was tested to identify those that could stimulate significant T cell response by PBMC in HLA-A02 seropositive humans. Using this approach, 10 peptides were identified that were recognized by HLA-A02 PBMC from seropositive humans herein. These were: one from SAG2C₃₈₋₄₆ (FLSLSLLVI (SEQ ID NO: 11)); one from SAG2D₁₈₀₋₁₈₉ (FMIAFISCFA (SEQ ID NO: 12)); two from SAG2X (SAG2X₄₄₋₅₂, FVIFACNFV (SEQ ID NO: 16); 39-40SAG2X₃₅₁₋₃₅₉, FMIVSISLV (SEQ ID NO: 13)); two from SAG3 (SAG3₃₇₅₋₃₈₃, FLLGLLVHV (SEQ ID NO: 15); SAG3_(136-144,) FLTDYIPGA (SEQ ID NO: 14)); two from sporozoite antigen SPA (SPA₁₂₋₂₀, ITMGSLFFV (SEQ ID NO: 17); SPA₈₂₋₉₀, GLAAAVVAV (SEQ ID NO: 18); one from MIC1₉₋₁₇ (VLLPVLFGV (SEQ ID NO: 20)); and one from MICA2P₁₁₋₁₉ (FAAAFFPAV (SEQ ID NO: 19)). All these identified peptides stimulated significant IFN-γ production by peripheral blood cells from 4 HLA-A*0201 persons infected with T. gondii, but not from 4 seronegative controls.

MHC Binding Assay Demonstrates A2-Supertype Binding Capacity of Peptides Recognized by HLA A2 Positive PBMCs.

The binding affinity of these identified peptides for MHC A2 molecules was proven empirically with a MHC binding assay. All of the peptides identified herein were bound with high affinity to the HLA-A02, all binding 4 or more alleles within the respective supertype except one binding 2 alleles. There are nine out of ten peptides that have HLA-A*0201 binding affinity that bound with a K_(d) of less than 50 nM. Specifically, SAG2X₄₄₋₅₂, SAG2X₃₅₁₋₃₅₉, SPA1₁₂₋₂₀, and MICA2P₁₁₋₁₉ bound with a K_(d) of 50 nM or less for all five tested HLA-A02 alleles. SAG3₃₇₅₋₃₈₃, SAG3₁₃₆₋₁₄₄, SPA12-20, and MIC1₉₋₁₇ bound 4 HLA-A02 alleles with affinities under 50 nM. SAG2C₃₈₋₄₆ bound HLA-A*0201 with >50 nM affinity, but bound HLA-A*0202 and HLA-A*0203 allele in the 50 to 500 nM range (intermediate binding). The data shows that all these identified peptides bound proteins of the HLA-A02 supertype as predicted, which would be predictive of candidates for eliciting IFN-γ from CD8⁺ T cells.

CD8⁺ T Cell Responses Against Peptides After Immunization in HLA Transgenic Mice.

To determine whether the peptides identified were immunogenic in vivo, HLA-A*0201 transgenic mice were immunized with pools of peptides that included peptides identified above as well as three other CD8⁺ T-cell epitopes, VVFVVFMGV (GRA6₂₄₋₃₂) (SEQ ID NO: 1), FMGVLVNSL (GRA6₂₉₋₃₇) (SEQ ID NO: 2), and FLVPFVVFL (GRA3₂₅₋₃₃) (SEQ ID NO: 3). A summary of peptide binding and immunogenicity activity is provided in Table 1. HLA-A*0201 transgenic mice were immunized with; (1) CD8⁺ epitope peptide pools, (2) CD8⁺ epitope peptide pools plus PADRE, and (3) CD8⁺ epitope peptides pool plus PADRE emulsified with GLA-SE. Eleven to fourteen days post immuniztion, spleen cells were isolated and exposed to each individual peptide. A peptide was considered immunogenic if it induced IFN-γ spot formation that was significantly higher in the immunization group when compared with the group immunization with PBS. After the immunizations with the two pooled peptides, SAG2C₃₈₋₄₆ (FLSLSLLVI (SEQ ID NO: 11)) and SAG2D₁₈₀₋₁₈₉ (FMIAFISCFA (SEQ ID NO: 12)) stimulated T cells from immunized HLA-A*0201 transgenic mice to produce significant IFN-γ production in vitro. However, when PADRE, a universal CD4⁺ epitope peptide, was added to the immunizing peptides, five peptides (SAG2C₃₈₋₄₆ FLSLSLLVI (SEQ ID NO: 11); SAG2D₁₈₀₋₁₈₉ FMIAFISCFA (SEQ ID NO: 12); SAG2X₄₄₋₅₂ FVIFACNFV (SEQ ID NO: 16); SAG2X₃₅₁₋₃₅₉ FMIVSISLV (SEQ ID NO: 13); SAG3₃₇₅₋₃₈₃ FLLGLLVHV (SEQ ID NO: 15)) induced significant IFN-γ production from T cells of immunized mice. More strikingly, all peptides except GRA6₂₄₋₃₂ (VVFVVFMGV (SEQ ID NO: 1)) and MICA2P₁₁₋₁₉ (FAAAFFPAV (SEQ ID NO: 19)) were found to be immunogenic when MLA also was used as an adjuvant to immunize HLA-A*0201 mice. To assess relative contributions of CD8⁺ T cells to overal IFN-γ response, the activity of splenic CD8⁺ T cells was blocked using antibody specific to the CD8⁺ T cell receptor. IFN-γ spot formation was significantly reduced in the presence of antibody to CD8 incubated with the spleen cells from mice immunized with the pooled peptides plus PADRE and MLA when the cells were stimulated by all of the peptides except GRA6₂₄₋₃₂ and MICA2P₁₁₋₁₉.

Peptide Immunizations are Protective Against Toxoplasma Challenge in HLA-A*0201 Transgenic Mice.

The epitopes that were identified could confer protection against parasite challenge in HLA-A*0201 mice. Groups of HLA-A*0201 mice (n=5-9 mice per group) were immunized with peptide pools with PADRE emulsified in MLA. Mice injected with PBS served as controls. Ten days after the second immunization, mice were challenged with 10,000 type II Prugniaud (Pru) strain that expresses the Firefly luciferase (FLUC) gene and imaged at 7 days post-challenge using the in vivo imaging system (IVIS; Xenogen, Alameda, Calif.) as previously described. Mice were imaged in ventral positions and photonic emissions were assessed using Living image® 2.20.1 software (Xenogen). Data were presented as pseudocolor representations of light intensity and mean photons/s/region of interest (ROI). The number of luciferase expressing parasites in the immunized HLA-A*0201 mice was significantly reduced compared to the unimmunized mice. A majority, 4 of 5 (80%) mice immunized with the peptides plus PADRE emulsified in MLA adjuvant survived parasite challenge (One mouse died between days 7 and 9.). In contrast, only 1 of 5 (20%) unimmunized mice survived parasite challenge (Three mice died between days 7 and 9 and one mouse died between days 9 and 11).

Population Coverage Prediction

An algorithm was developed to calculate projected population coverage of a T cell epitope-based vaccine using MHC binding or T cell restriction data and HLA gene frequencies. This web based tool found by Vita R et al. (2010), was used to predict population coverage of these HLA-A02 epitope peptides based vaccines. The population coverage calculation results showed that the population coverage is varied in different regions: these peptides covered 23.82% population in Australia; 47.01% in Europe; 26.87% in North America; 39.29% in South America; 21.40% in North-East Asia; 12.35% in South-East Asia; 26.78% in Oceania; and 18.27% in Sub-Saharan Africa; and 40.36% for others. The average population coverage is 25.61%±13.31%

Discussion

Eleven T. gondii protein amino acid sequences were screened for CD8⁺ T cell epitopes by using an HLA motif algorithm to predict potential epitopes corresponding to the HLA-A02 supertype family, which is represented in 47% of the Europeans and 25% of the world population. Peptides were screened from tachyzoite, bradyzoite or sporozoite proteins which were either seen to elicit immune response or were known to be secreted and present in the cytoplasm and thus able to access the MHC Class I pathway. These proteins included GRA10, GRA15, SAG2C, SAG2D, SAG2X, SAG3, SRS9, BSR4, SPA, MIC1 or MICA2P of the type II T. gondii strain, ME49, whose sequences came from the ToxoDB website http://toxodb.org/toxo/. These peptides were further selected based on a high MHC allele binding score in a bioinformatic analysis (IC₅₀<50 nM). Ten nonamer or decamer peptides derived from the amino acid sequence of SAG2C, SAG2D, SAG2X, SAG3, SPA, MIC1, and MICA2P were identified via ELISpot assays with peripheral blood mononuclear cells from HLA-A*0201 T. gondii-seropositive individuals. In addition, we included three peptides for analysis that had earlier been identified from VVFVVFMGV (GRA6₂₄₋₃₂) (SEQ ID NO: 1), FMGVLVNSL (GRA6₂₉₋₃₇) (SEQ ID NO: 2), FLVPFVVFL (GRA3₂₅₋₃₃) (SEQ ID NO: 3). HLA-A*0201 transgenic mice immunized with these peptide pools plus adjuvant could induce peptide-specific high IFN-γ production and protect mice against challenge from type II parasites.

The peptide epitopes reported here to elicit IFN-γ are primarily derived from SAG2, SPA and MIC proteins of type II T. gondii. Sequence analysis demonstrated that the SAG1 related sequence (SRS) protein family that is expressed in a stage-specific manner is divided into two major branches, the SAG1-like sequence family and SAG2-like sequence family (Jung C et al., 2004). The tachyzoite surface is dominated by SAG2A, SAG3, SRS 1, SRS2, and SRS3. Some of these proteins have been shown to be involved in invasion and attachment. SAG3 was considered as one member of the redundant system of T. gondii receptors that act as ligands mediating host cell recognition and attachment (Dzierszinski F. et al., 2000). Two peptides, FLLGLLVHV (SEQ ID NO: 15) and FLTDYIPGA (SEQ ID NO: 14), derived from SAG3₃₇₅₋₃₈₃ and SAG3₁₃₆₋₁₄₄ were identified as epitopes that elicit IFN-γ from CD8⁺ T cells. HLA-binding assay demonstrates that these two peptides have good binding affinity for the HLA-A*0201 supertype. Not only do they have a high binding affinity for HLA-A*0201 allele, but they also bound well to three or four other HLA-A02 alleles.

SAG2C, -D, -X, -Y, encoding bradyzoite surface molecules belonging to the SAG2 family are important for persistence of cysts in the brain. A significantly lower cyst number was seen in mice infected with Pru ΔSAG2CDXY parasites (Saeij et al., 2005). There was one peptide disclosed herein derived from SAG2C₃₈₋₄₆, one peptide derived from SAG2D₁₈₀₋₁₈₉, and two peptides derived from SAG2X₄₄₋₅₂ and SAG2X₃₅₁₋₃₅₉ that elicited IFN-γ production from CD8⁺ T cells from seropositive HLA-A02 individuals, but not seronegative HLA-A02 persons. HLA-binding assay demonstrated that these peptides have good binding affinity for five HLA-A02 alleles, except SAG2C₃₈₋₄₆ which only bound two alleles with affinity ≦50 nM.

The complete life cycle of T. gondii encompasses both the sexual stage (sporozoite) and asexual stage (tachyzoite and bradyzoite). Of the three, the infective stage of T. gondii, sporozoites in oocysts are resistant and persist in the environment after excretion by cats. Sporulation creates highly infectious oocysts that have been linked to large scale outbreaks of toxoplasmosis. Sporozoite surface antigen (SPA) is the dominant surface coat protein expressed on the surface of sporozoites. Two peptides derived from this protein, SPA₁₂₋₂₀ and SPA₈₂₋₉₀, were found to have the ability to stimulate human CD8⁺ T cells to produce IFN-γ and bound with high affinity all the tested HLA-A02 supertype allele peptides.

MIC1-3 knockout T. gondii was considered as a good candidate for a vaccine against T. gondii-induced abortion in sheep and although MIC knockout parasites could be a vaccine, MICs have been found to be immunogenic in mice. Herein, two peptides MIC1₉₋₁₇ and MICA2P₁₁₋₁₉ which have high binding affinity for HLA-A02 supertype were identified as CD8⁺ T cell epitopes that could elicit IFN-γ from T. gondii seropositive HLA-A02 persons. However, MICA2P₁₁₋₁₉ was not found to be immunogenic in HLA-A*0201 transgenic mice even when GLA-SE was used as an adjuvant.

The relationship between A2 binding affinity and the immunogenicity of a series of A2 motif-containing peptides has been examined previously (Sette et al. 1994; Rapin et al. 2010; Kubo et al. 1994). MHC affinity plays an important role in determining immune responsiveness. Only peptides with a relatively high binding affinity for MHC of 500 nM or less usually are immunogenic. All the identified peptides have binding affinities lower than 500 nM with 11 out of 13 peptides exhibiting very high A2 binding affinities.

Furthermore, epitopes selected from many gene products increase the breadth of the immune response. The combination of more epitopes from different proteins can make immunization more robust and broaden its coverage. Inclusion of epitopes derived from bradyzoites and sporozoites can control against bradyzoites from cysts or against sporozoites from oocysts early during acquisition of infection. T cells effective against bradyzoite epitopes can reduce number of bradyzoites immediately upon cyst rupture. Thus, these enhance the biologically relevant efficacy in humans as well as reach higher population coverage.

These peptides were proven to be immunogenic when these peptides were formulated with a universal CD4⁺ peptide, PADRE and adjuvants for immunization of HLA-A*0201 transgenic mice. PADRE, a synthetic nonnatural Pan HLA DR binding epitope peptide that binds promiscuously to variants of the human MHC Class II molecule DR and murine Class II, and is effective in human and HLA transgenic mice, can augment CD8⁺ T cell effector functions by inducing CD4⁺ T helper cells. Spleen cells from mice immunized with peptides alone cannot activate T cells to secrete IFN-γ, but when the CD4⁺ T helper cell epitope PADRE was added in the immunogen, the secretion of peptide-specific IFN-γ was elicited. This indicated that the PADRE epitope delivers help for a MHC Class I restricted peptide-specific CTL response to T. gondii. Our results suggest that in a vaccine to prevent T. gondii infection, both CD4⁺ and CD8⁺ epitopes are preferably be targeted in order to drive a protective immune response.

However, low-molecular-weight synthetic peptide antigens are not highly immunogenic by themselves. 3-deacylated monophosphoryl lipid A (GLA-SE) is a detoxified derivative of the lipopolysaccharide (LPS) from Salmonella minesota R595, which is a Toll-like receptor 4 (TLR4) agonist and thus a potent activator of Th1 responses. A robust response was observed when MLA was included in this preparation used to immunize mice. High amounts of IFN-γ production were elicited from mice immunized with pooled peptides plus PADRE and MLA when the spleen cells were stimulated by the individual peptides, and the immunized mice were subsequently protected against high parasite burden with type II parasite challenge and had a significantly enhanced survival rate.

Disclosures herein provide not only a conceptual foundation, but reagents and proof of principle in terms of protection.

Focus included the identification of HLA-A02-specific epitopes by selecting and testing peptides based on HLA-A*0201 binding motif. Thirteen peptides were identified via ELISpot assays with peripheral blood mononuclear cells from HLA-A02 seropositive persons. Eleven peptides with the help of CD4⁺ T cell epitopes and adjuvancy of GLA-SE were proven to be immunogenic in transgenic mice using an assay measuring ability to elicit IFN-γ and protect the mice against parasite challenge.

Construction of CD4-CD8 Peptides Based Candidate Vaccine

CD8⁺ T cell epitopes were identified from Toxoplasma gondii proteins, based on their significant recognition by T cells from T. gondii seropositive HLA-A*1101 individuals. A universal CD4⁺ T cell epitope, PADRE (AKFVAAWTLKAAA (SEQ ID NO: 7)), was linked in sequence with the N-terminal end of one of the three different T. gondii CD8⁺ T cell epitopes: KSFKDILPK (SAG1₂₂₄₋₂₃₂) (SEQ ID NO: 4), AMLTAFFLR (GRA6₁₆₄₋₁₇₂) (SEQ ID NO: 5), RSFKDLLKK (GRA7₁₃₄₋₁₄₂) (SEQ ID NO: 6) and these three epitopes linked together with three alanines as the linker. The N-terminal end of each resulting CD4-CD8 peptide was extended by a lysine covalently linked to two molecules of the palmitic acid moiety. The lipopeptides (Lp) were named as LpKS9, LpAM9, LpRS9 and LpKS9/AM9/RS9 which are shown in FIG. 2.

Immunogenicity of Lipopeptides in HLA-A*1101 Transgenic Mice

HLA-A*1101 transgenic mice were immunized twice at three week intervals with lipopeptides which were dissolved in PBS. Two weeks after the last immunization, the spleens were removed from immunized mice and the ability of splenocytes to produce IFN-γ upon the stimulation of peptides was analyzed. Transgenic mice immunized with the three single peptide lipopeptide vaccines had T cells that produced IFN-γ (FIG. 2B). The lipopeptide vaccine LpKS9 and LpAM9 stimulated higher IFN-γ production than LpRS9. However, LpKS9/AM9/RS9 with three peptide epitopes linked together did not stimulate strong IFN-γ responses when splenocytes from these mice were exposed to each of the individual peptides in vitro.

Comparison of Vaccination with Different Formulations of Peptides

In order to determine which formulation was most immunogenic, vaccination with a single peptide or a mixture of the peptides was compared with linked lipopeptide vaccines. Mice immunized with a vaccine formulated with a single peptide SAG¹ ₂₂₄₋₂₃₂, KS9/PADRE with the adjuvancy of MLA and Pam₂Cys, elicited IFN-γ production (SFC:248±65; mean±SEM) four-fold higher (p<0.01) than mice that received LpKS9/MLA vaccination (63±17). Similar results, with substantial IFN-γ production, were found when splenocytes from mice immunized with a mixture of peptides and adjuvants which were compared with IFN-γ production by splenocytes from mice immunized with lipopeptide vaccines constructed with the three peptides linked together with alanine spacers LpKS9/AM9/RS9. However, significant IFN-γ production was only present with KS9 and AM9 stimulation of spleen cells, and was not present when the spleen cells were stimulated by RS9 peptide.

Effects of Adjuvant on Immunogenicity of Pooled Peptide Vaccination

To determine how adjuvants effected immunogenicity of these peptides, HLA-A*1101 transgenic mice were immunized with pools of peptides that included all of the three peptides (KS9, AM9, RS9) alone or with varying adjuvants. HLA-A*1101 transgenic mice were immunized with: (1) CD8⁺ epitope peptide pool, (2) peptide pool plus PADRE, (3) peptide pool plus PADRE emulsified with MLA, and (4) peptide pool plus PADRE and Pam₂Cys emulsified with MLA. Mice were inoculated three times at two weeks intervals. Eleven to fourteen days post immunization, spleen cells were isolated and exposed to each individual peptide. A peptide was considered immunogenic if it induced IFN-γ spot formation that was significantly higher in the immunization group compared with the group inoculated with PBS. After the immunizations, only KS9, AM9 were found to be immunogenic in HLA-A*1101 transgenic mice when the CD4⁺ helper T cell peptide epitope was included. Robust responses were observed when MLA was added in the vaccine. Greater responses were elicited when Pam₂Cys was used as an adjuvant for some but not all the peptides.

Vaccination with Peptide Pools and Adjuvants Protects Mice Against Type II Parasite Challenge

HLA-A*1101 transgenic mice were immunized with peptide pools plus PADRE and Pam₂Cys in MLA three times at two week intervals because it was the most immunogenic. Mice were challenged 2 wks after the last immunization. They were imaged 7 days post-challenge with 10,000 Pru (Fluc) using the Xenogen in vivo imaging system. The numbers of luciferase expressing parasites in immunized HLA-A*1101 transgenic mice were significantly reduced compared to the numbers of parasites in unimmunized mice.

Identification of New Candidate T. gondii Specific HLA-A*1101-Restricted Epitopes

Three epitopes were identified that provided protection against parasite challenge. As a next generation vaccine additional HLA-A11 epitopes were identified to be used for vaccine development. In order to identify additional peptides from T. gondii that were present in tachyzoites, bradyzoites, and sporozoites of Type II strains for HLA-A03 supertype restricted CD8⁺ T cells, candidate peptides were screened from tachyzoite, bradyzoite and sporozoite proteins (GRA15, GRA10, SAG2C, SAG2X, SAG3, SRS9, SPA and MIC) of the Type II T. gondii strain (Table 2a). Peripheral blood mononuclear cells from seropositive T. gondii donors were tested for response to these peptides by using the IFN-γ ELISpot assay. Pooled peptides were tested initially and Pools 2 and 5 were significantly different (p<0.05) from the control. Then the individual peptides were tested. Three out of 34 epitopes elicited responses greater than 50 IFN-γ SFC from seropositive donors PBMC cells. They are derived from STFWPCLLR (SAG2C₁₃₋₂₁) (SEQ ID NO: 21); SSAYVFSVK (SPA₂₅₀₋₂₅₈) (SEQ ID NO: 22); and AVVSLLRLLK (SPA₈₉₋₉₈) (SEQ ID NO: 23). All peptides identified herein show high binding affinity to three to five HLA-A03 supertype alleles in the MHC-peptide binding assay (Table 2b).

Vaccination with Peptide Pools Including Newly Identified Peptides and Adjuvants Provide More Protection to Mice Against Type II Parasite Challenge

HLA-A*1101 transgenic mice were immunized with peptide pools that include: KSFKDILPK (SAG1₂₂₄₋₂₃₂) (SEQ ID NO: 4); AMLTAFFLR (GRA6₁₆₄₋₁₇₂) (SEQ ID NO: 5); RSFKDLLKK (GRA7₁₃₄₋₁₄₂) (SEQ ID NO: 6); STFWPCLLR (SAG2C₁₃₋₂₁) (SEQ ID NO: 21); SSAYVFSVK (SPA₂₅₀₋₂₅₈) (SEQ ID NO: 22); AVVSLLRLLK (SPA₈₉₋₉₈) (SEQ ID NO: 23) plus PADRE and Pam₂Cys in MLA three times at two week intervals. Significant IFN-γ spot formation responses were observed in vitro by the cells from immunized mice exposed to all the peptides except GRA7₁₃₄₋₁₄₂. The inclusion of the newly identified peptides thus had potential to enhance immunogenicity in transgenic HLA-A*1101 mice.

Mice were challenged 2 weeks after the last immunization. They were imaged five days post-challenge with 10,000 Pru (Fluc) using Xenogen in vivo imaging system. The numbers of luciferase expressing parasites in immunized HLA-A*1101 mice were significantly reduced compared to the numbers of parasites in unimmunized mice.

Population Coverage Prediction

An algorithm was developed to calculate projected population coverage of a T cell epitope-based vaccine using MHC binding or T cell restriction data and HLA gene frequencies. This web-based tool, (Vita R, Zarebski L, Greenbaum J A, Emami H, Hoof I, Salimi N, Damle R, Sette A, Peters B. The immune epitope database 2.0. Nucleic Acids Res. 2010 January; 38(Database issue):D854-62. Epub 2009 Nov. 11), was used to predict population coverage of these HLA-A*03 supertype peptide epitopes-based vaccine. The population coverage calculation results indicate that such coverage is varied in different geographic regions: these peptides covered 28.90% population in Australia; 41.46% in Europe; 11.29% in North America; 18.86% in North-East Asia; 36.62% in South-East Asia; 37.73% in South-East Asia; 34.29% in South-West Asia; 34.09% in Oceania; 27.32% in North Africa; 13.14% in Sub-Saharan Africa and 22.13% for others. The average population coverage is 24.51%±12.06%.

Discussion

Immunization of HLA-A*1101 transgenic mice with either mixture of peptides or lipopeptides derived from three identified T. gondii specific HLA-A*1101 restricted CD8⁺ T cell epitopes emulsified in 3-deacylated monophosphoryl lipid A (MLA) adjuvant was evaluated. Immunization of transgenic mice with a mixture of CD8⁺ epitope peptide pools plus PADRE and adjuvants were able to induce splenocyte to produce IFN-γ to protect against challenge with high burden of Type II parasite.

Conjugation of CD8⁺ T cell determinants to lipid groups is known to enhance specific cell-mediated responses to target antigens in animals and humans, although mechanisms whereby immunity is achieved remains poorly understood. Lipopeptides hold several advantages over other conventional vaccine formulations; for instance, they are self-adjuvanting and display none of the toxicity-associated side effects of other Th1-inducing adjuvant systems. In the present disclosure, transgenic mice that were immunized with three short lipopeptide vaccines had T cells that produced IFN-γ. Among them the lipopeptide vaccine formulated with KS9 or AM9 stimulated higher IFN-γ production than the lipopeptide vaccine formulated with RS9. However, the lipopeptides with three epitope peptides linked together with alanine spacers did not stimulate an IFN-γ response by splenocytes from immunized mice when the splenocytes subsequently were exposed to each of the peptides in vitro. The reason why the lipopeptides with the three linked peptides did not work well in the transgenic mice might be related to the linker. The three linker “AAA” between the peptides had previously been demonstrated to result in sensitization to each of the linked peptides.

Because the three linked peptides in the lipopeptide formulation were not effective and a mixture of the components with a single peptide was as robust or more robust than the lipopeptide, the approach with the three peptides that had been included in the linked lipopeptide with the universal helper CD4⁺ T cell peptide, PADRE, and adjuvants was tried as described below. The response was robust both in vivo (FIG. 3) and in vitro.

Mice immunized with mixture of CD8⁺ and CD4⁺ epitope peptides and lipid Pam₂Cys emulsified in MLA elicited higher IFN-γ production than mice immunized with lipopeptides constructed with the same components of CD4⁺, CD8⁺, and Pam₂Cys. The approach using cocktails of non-covalently linked lipid mixed to HTL and CTL epitopes for simultaneous induction of multiple CTL specificities is preferred for some vaccine embodiments.

HTL responses are preferred for the development of CTL responses, at least in the case of lapidated covalently or non-covalently linked HTL-CTL epitope constructs formulated in PBS. Several previous studies have illustrated a role for CD4⁺ responses for development of CD8 CTL responses, both in human and in experimental animals. The inclusion of PADRE, a synthetic peptide that binds promiscuously to variants of the human MHC class II molecule DR and is effective in mice, also augmented CD8⁺ T cell effector functions by inducing CD4⁺ T helper cells. Both CD4⁺ and CD8⁺ epitopes were targeted in order to drive a protective immune response.

Adjuvanting antigens contributes to the success of vaccination. An example herein is that 3-deacylated monophosphoryl lipid A (MLA), a detoxified derivative of the lipopolysaccharide (LPS) from Salmonella minesota R595 was a potent adjuvant. This is a Toll-like receptor 4 (TLR4) agonist and thus a potent activator of Th1 responses. It has been used as an adjuvant in human vaccine trials for several infectious disease and malignancy indications. It has been very effective as an adjuvant providing CD4⁺ T cell help for immunizations against other protozoan infections such as leishmaniasis. A robust response was observed when MLA was included in preparation for immunization of mice. Pam₂Cys (S-[2,3-bis(palmitoyloxy)propyl]cysteine) is a lipid component of macrophage-activating lipopeptide. Pam₂Cys binds to and activates dendritic cells by engagement of Toll-like receptor 2 (TLR-2). Toll-like receptors (TLRs) function as pattern-recognition receptors in mammals. It is suggested that both TLR2 and TLR4 receptors might participate in the host defense against T. gondii infection through their activation by the GPIs and could work together with other MyD88-dependent receptors, like other TLRs, to elicit an effective host response against T. gondii infection. In our study, there was a slightly more robust response observed when Pam₂Cys was co-administered for some peptide.

HLA-restricted epitopes from Toxoplasma gondii have been evaluated and shown to provide protection against parasite challenge. Various peptide-based approaches to induction of IFN-γ responses were evaluated as part of ongoing efforts to develop immunosense vaccines for use in humans. Robust protection was achieved in the HLA-A*1101 transgenic mice challenged with type II parasites following immunizations. In order to identify additional peptides from T. gondii that were present in tachyzoites or bradyzoites or sporozoites of Type I and II strains and elicited IFN-γ from HLA-A03⁺ supertype (which includes the HLA*1011 alelle) restricted CD8⁺ T cells, bioinformatic algorithms were utilized to identify novel, T. gondii-derived, epitopes restricted by the HLA-A03 supertype. Then PBMC cells were tested to determine whether the peptides elicited IFN-γ from human CD8⁺ T cells from seropositive persons. This was intended to collectively provide broad coverage for the human population with HLA-A03 supertype worldwide. The additional peptides identified as immunogenic for human peripheral blood cells were also robust in eliciting IFN-γ and when used to immunize mice.

III. Cellular Immunogenicity of Two Identified B7 Restricted CD8⁺ T Cell Epitope Peptides in HLA B*0702 Transgenic Mice.

To address the capacity of two identified B7 epitopes, GRA7₂₀₋₂₈ (LPQFATAAT (SEQ ID NO: 8)) and GRA3₂₇₋₃₅ (VPFVVFLVA (SEQ ID NO: 9)), to prime for IFN-γ responses, HLA-B07 transgenic mice were immunized s.c. with each of peptides alone and peptides with PADRE or peptides with PADRE and Pam₂Cys. Each of these regents was mixed with MLA. A mixture of these two peptides with PADRE, or plus Pam₂Cys mixed with MLA were also used as immunogens. Little IFN-γ responses were observed following immunization by peptides mixed with MLA alone. When PADRE was added for immunization, a significant amount of IFN-γ was produced following stimulation by one B7 epitope peptide LT9 (LPQFATAAT (SEQ ID NO: 8)) in vitro (P=0.0003, compared to peptide mixed with MLA alone). An even more robust response was achieved when Pam₂Cys was added to the immunogen. In contrast, no significant amount of IFN-γ was produced using splenocyte groups immunized with another B7 epitope peptide VA9 (VPFVVFLVA (SEQ ID NO: 9)) (P>0.05, compared to control group), when they were stimulated by this peptide.

Similar results were found with peptide pool immunizations. Splenocytes from the mice immunized with the mixtures of two peptides LT9 and VA9 with PADRE or plus Pam₂Cys mixed with MLA produced significant amount of IFN-γ when stimulated by LT9 (P<0.001, compared to the PBS immunization group), but not by VA9 (P>0.05, compared to the PBS immunization group).

To assess relative contributions of CD8⁺ T cells to overall IFN-γ response, the activity of splenic CD8⁺ T cells was blocked using antibody specific to the CD8⁺ T cell receptor. IFN-γ spot formation was significantly reduced in the presence of αCD8 incubated with the spleen cells from mice immunized with LT9 included in the vaccination and stimulated by LT9.

Relation Between Solubility and Immunogenicity

The correlation between the solubility of the peptides and their immunogenicity is summarized in Table 4. The VA9 was much less soluble with overall percent solubility of 10%. In contrast, LT9 had 99% solubility. LT9 was effective in the peptide vaccine construct, but VA9 was not. Reduced solubility of this peptide in the vaccine correlated with its reduced immunogenicity.

Evaluation of Cellular Immune Responses to LT9 Formulated Peptide Vaccine

Since VA9 peptide formulation vaccination of HLA-B*0702 transgenic mice could not effectively elicit CD8⁺ T cell to produce IFN-γ, only LT9 peptide formulations were evaluated for protection in HLA-B07 transgenic mice in subsequent studies.

The ability of MLA and Pam₂Cys to adjuvant the LT9 peptide also was evaluated. Mice were immunized with LT9 peptide alone, LT9/PADRE, LT9/PADRE/MLA, LT9/PADRE/MLA/Pam₂Cys. Immunization with LT9 alone did not induce effective IFN-γ production, but when the PADRE helper epitope was included in the immunogens, it induced a small amount of IFN-γ but this was not significant (P=0.057, when compared to peptide alone). When MLA was added, robust CD8⁺ T cell production of IFN-γ was achieved (P=0.0001, compared to peptide alone; P=0.00013 compared to peptide/PADRE). Greater responses were observed when Pam₂Cys was added in the vaccine (P=0.000009, compared to peptide alone; P=0.000013, compared to peptide/PADRE; P=0.09, compared to peptide/PADRE/MLA). However, the addition of Pam₂Cys to PADRE/MLA did not significantly enhance the LTP specific IFN-γ response. Thus, MLA is an effective adjuvant to enhance IFN-γ production in response to CD8⁺ T cell eliciting peptides in HLA-B*0702 transgenic mice.

LT9-specific proliferative responses with a SI of ˜3.5 were observed following immunization with LT9/PADRE/MLA/Pam₂Cys. When the same peptide epitope was used alone for immunization, SI was 1.5. The magnitude of lymphocyte blastogenesis and IFN-γ elicited by LT9 with adjuvants had the same patterns.

PADRE Delivers Help for Peptide-Specific CTL Response

In order to determine function of the CD4⁺ T cell epitope PADRE in this peptide vaccine, PADRE-specific T cell responses were evaluated by IFN-γ ELISPOT assay and a proliferative response assay using splenocytes from the immunized mice. Immunization with the CD8⁺ T cell epitope alone did not induce an IFN-γ response, whereas when the CD4⁺ T cell epitope PADRE was added to the immunogen, CD8⁺ T cells could be activated to secrete IFN-γ (P=0.0006 compared to PBS group; P=0.001 compared to peptide alone immunized group). A proliferative response of SI ˜4, was observed following immunization with LT9 plus PADRE and Pam₂Cys in MLA. However, blocking the CD4⁺ T cell receptor using anti-CD4⁺ antibody significantly reduced IFN-γ production, thus indicating that PADRE is an effective CD4⁺ Th epitope which contributes to the peptide vaccine construct. However, in some instances, PADRE elicited only a small enhancement of the response to LT9.

LT9 Peptide Elicited HLAB7-Restricted CD8⁺ T Cells Responses in Immunized Mice.

Splenocytes were isolated from peptide-immunized HLA-B07 transgenic mice 10 days after immunization and incubated with antibodies to αCD8 or HLA-B07 and their common isotype control prior to stimulation with LT9. Their abilities to generate IFN-γ and lymphocyte proliferation in response to peptide were tested. To study the ability of αHLA-B*0702 to block response of CD8⁺ T cells in the same experiment, blocking αCD8 T cells and blocking αHLA-B*0702 were used with the same spleen cells in the same experiment. The data shows that blocking CD8⁺ T cell receptors using αCD8⁺ antibody significantly reduced LT9-specific IFN-γ production and T cell proliferation (P<0.05).

Then, to further analyze the association of LT9 presentation by HLA-B*0702, blocking experiments using a monoclonal anti-HLA-B*0702 antibody (BB7.2) was performed. Results indicated that the IFN-γ secretion was significantly decreased by the anti-HLA-B07 antibody but not by the control antibody (p<0.05). These results demonstrate that the peptide specific IFN-γ response is HLA-B*0702 restricted and involves CD8⁺ T cells. The partial blocking by the HLA B7 antibody is likely a function of the antibody's capacity for blocking, and not reactivity of the peptide with the murine H2 haplotypes. This is because the algorhithms predict poor affinity of all of the background Balb/c and B6 H2 molecules with these peptides. Using the IEDB to predict, these peptides are predicted to bind poorly to these H-2 molecules.

Peptide with Adjuvant Vaccination Protects Mice Against Type II Parasite Challenge

HLA-B*0702 transgenic mice were immunized with the LT9 peptide plus PADRE and Pam₂Cys in MLA three times at two week intervals. Mice were challenged 2 weeks after the last immunization. They were imaged 5 days post-challenge with 10,000 Pru (Fluc) using the Xenogen in vivo imaging system. The numbers of luciferase expressing parasites in immunized HLA-B*0702 mice were significantly reduced compared to the numbers of parasites in unimmunized mice. There was also a significant reduction of cysts in the brain when mice were immunized with LT9 peptide vaccine. There was a 54% reduction from a mean of 335 to 155 cysts per brain.

Discussion

Herein, two T. gondii-specific HLA-B*07 restricted CD8⁺ T cell epitopes LT9 (LPQFATAAT (SEQ ID NO: 8)) and VA9 (VPFVVFLVA (SEQ ID NO: 9)) derived from GRA7₂₀₋₂₈ and GRA3₂₇₋₃₅ elicited IFN-γ from human PBMC cell, 4 HLA-B07 seropositive and 0 of 3 seronegative persons. Upon immunization of mice, only LPQFATAAT (SEQ ID NO: 8) elicited CD8⁺ T cell specific IFN-γ with the help of a universal CD4⁺ epitope and adjuvants, MLA and Pam₂Cys, enhanced the response. This peptide vaccine plus adjuvants protect HLA-B07 transgenic mice from type II parasite challenge.

CD8⁺ T cell epitopes identified were from dense granule (GRA) proteins of Toxoplasma gondii. Many studies have shown that dense granule antigens (GRA) are involved in parasite survival and virulence (Mercier C, et al. (2005). The proteins are secreted in abundance and circulate in the blood stream during the first hours following infection and appeared 2-5 days after mice infected with parasite. The GRA proteins have thus been considered to be attractive vaccine candidates for the prevention and control of toxoplasmosis.

Two peptides were recognized by T cells from T. gondii specific HLA-B07 restricted PBMC. However, although peptide VPFVVFLVA (SEQ ID NO: 9) was recognized by T cells from Toxoplasma gondii-specific HLA-B07-restricted human PBMC, it did not induce a significant IFN-γ response in HLA-B*0702 transgenic mice. We therefore concluded that VA9 was presented by HLA-B07 supertype molecules to CD8⁺ T cells in humans, but was not present in significant quantity to be presented by HLA-B07 supertype molecules to CD8⁺ T cells in the transgenic mice. This seems most likely to be due to the relative insolubility of the VA9 peptide. The VA9 peptide was 90% insoluble with overall percent solubilities of 10% in PBS. In contrast, LT9 was soluble, with 99% solubility in PBS. LT9 was effective in the peptide vaccine construct, but VA9 was not, reduce solubility of peptides in the vaccine peptides might correlate with reduced immunogenicity.

The inclusion of PADRE, a synthetic nonnatural Pan HLA DR binding Epitope peptide that binds promiscuously to variants of the human MHC Class II molecule DR and is effective in human and HLA transgenic mice, can augment CD8⁺ T cell effector functions by inducing CD4⁺ T helper cells. The PADRE epitope was demonstrated to deliver help for a MHC Class I restricted peptide-specific CTL response to the T. gondii peptide herein. Preference for CD4⁺ T cell help in the generation of a CD8⁺ T cell response also has been proved in viral, bacterial, and parasite models. In studies of Trypanosoma cruzi infections (Padilla A, et al. 2007), it was demonstrated that CD4⁺ T cell help is required during the primary response to immunodominant epitopes. In a vaccine, both CD4⁺ and CD8⁺ epitopes should be targeted in order to drive a protective immune response.

Although peptide vaccines including CD4⁺ and CD8⁺ epitopes could prime cell-mediated immune responses, low-molecular-weight synthetic peptide antigens are not highly immunogenic by themselves. These observations have led to investigations to co-administer adjuvants with vaccine antigens to potentiate activity of vaccines and the weak immunogenicity of the synthetic epitopes. Adjuvanting antigens contribute to the success of vaccination 3-deacylated monophosphoryl lipid A (MLA) a detoxified derivative of the lipopolysaccharide (LPS) from Salmonella minesota R595 which is a Toll-like receptor 4 (TLR4) agonist and thus a potent activator of Th1 responses. It has been used as an adjuvant in human vaccine trials for several infectious diseases and cancer. It has been very effective as an adjuvant providing CD4⁺ T cell help for immunizations against other protozoan infections such as leishmaniasis. In our study, a robust response was observed when MLA was included in preparation for immunization of mice. Pam₂Cys (S-[2,3-bis(palmitoyloxy)propyl]cysteine) is a lipid component of macrophage-activating lipopeptide. Pam₂Cys binds to and activates dendritic cells by engagement of Toll-like receptor 2 (TLR-2). Toll-like receptors (TLRs) function as pattern-recognition receptors in mammals. It is suggested that both TLR2 and TLR4 receptors might participate in the host defense against T. gondii infection through their activation by the GPIs and could work together with other MyD88-dependent receptors, like other TLRs, to obtain an effective host response against T. gondii infection. In our study, an even more robust response was observed in the Pam₂Cys co-administration group and robust protection was achieved in the transgenic mice challenged with type II parasites following immunizations.

The work presented herein indicates that an HLA-B07 restricted epitope LT9 (LPQFATAAT (SEQ ID NO: 8)) derived from GRA7₂₀₋₂₈ that can elicit IFN-γ from T cells of seropositive HLA-B07 persons elicits IFN-γ and CD8⁺ T cells when administered with a universal DR epitope PADRE for CD4⁺ help and MLA and Pam₂Cys to adjuvant MHC Class I-restricted CD8⁺ T cells. This peptide vaccine reduced parasite burden in immunized mice challenged with type II parasites. This is the first report of a T. gondii specific HLA-B07 restricted CD8⁺ T cell epitope based vaccine that protects HLA-B07 transgenic mice against T. gondii.

Materials and Methods

I. Bioinformatic prediction of CD8⁺ T cell epitopes ARB, SMM, and ANN algorithms from the immunoepitope database (IEDB) http://www.iedb.org/ were used to predict binding affinity to HLA-A*0201 of T. gondii specific peptides. Protein sequences from GRA10, GRA15, SAG2C, SAG2D, SAG2X, SAG3, SRS9, BSR4, SPA, and MIC were screened for nonamer or decamer CD8⁺ T cell epitopes based on their predicted binding affinity to HLA-A*02 supertype molecules. A total of 29 unique peptides that had IC₅₀<50 nM using the bioinformatic algorithm were selected. Protein sequences were from ToxoDB 5.1. Population coverages of peptides were predicted as described in Bui H H, et al. (2007).

Peptides and GLA-SE

All peptides were synthesized by Synthetic Biomolecules (San Diego, Calif.) and were >90% pure. Peptides were first dissolved in DMSO and then diluted in PBS or media. GLA-SE mimetic was synthesized by Infectious Diseases Research Institute (IDRI, Seattle, Wash.).

MLA=GLA-SE

MHC-Peptide Binding Assays

Quantitative assays to measure binding of peptides to HLA Class I molecules are based on inhibition of binding of a radiolabeled standard peptide. Assays were performed as described in Cheng Y and Prusoff W H (1973) and Gulukota, K., et al. (1997). Briefly, 1-10 nM of radiolabeled peptides were co-incubated with 1 M-1 nM purified MHC and 1-3 μM human β₂-microglobulin. After 2 days, binding of radiolabeled peptide to corresponding MHC Class I molecule was determined by capturing MHC-peptide complexes on Greiner Lumitrac 600 microplates coated with W6/32 antibody and measuring bound counts per minutes using a Topcount microscintillation counter. Concentration of peptide yielding 50% inhibition of binding of radiolabeled probe peptide (IC₅₀) then was calculated. Under conditions used, where [radiolabeled probe]<[MHC] and IC₅₀≧[MHC], measured IC₅₀ values are reasonable approximations of true K_(d) values.

Mice

HLA-A*0201 K_(d) transgenic mice were produced at Pharmexa-Epimmune (San Diego, Calif.) and bred at the University of Chicago. All studies were conducted with Institutional Animal Care and Use Committee at the University of Chicago approval.

Enzyme-Linked Immunospot (ELISpot) Assay

Cryopreserved peripheral blood mononuclear cells (PBMC), obtained in accordance with institutional and NIH guidelines, from both T. gondii-seropositive and seronegative individuals were used in ELISpot assays to study human PBMCs. PBMCs were isolated from heparinized blood samples by density gradient centrifugation using Histopaque (Sigma-Aldrich), then washed twice with PBS, and cryopreserved in AIM-V medium (Gibco) containing 20% FCS and 10% DMSO.

2×10⁵ PBMCs per well were incubated at 37° C., 5% CO₂ in AIM-V medium, pulsed by peptide or peptide pools at 10 μg/ml in MSIPS4W10 Multiscreen HTS-IP 96-well plates (Millipore, Bedford, Mass.) previously coated with 50 μl of 15 μg/ml anti-human IFN-γ (1-D1K) monoclonal antibody (mAb) in sterile PBS overnight, and then processed as described in Tan T G et al. (2010). After washing with sterile PBS and blocking with RPMI-1640 medium containing 10% FCS at room temperature for 2-3 hr, plates were successively incubated with 100 μl of 1 ng/ml biotinylated anti-human IFN-γ mAb (7B6-1) for 2 hr and streptavidin-conjugated alkaline phosphatase at a 1:1000 dilution for 1 hr at room temperature. Wells were washed with PBS between incubation stages. Spots were developed using 5-bromo-4-chloro-3-indolyl-phosphate/p-nitro blue tetrazolium chloride (BCIP/NBT) and quenched by extensive washing with distilled water. After drying, plates were counted using an automated ELISpot reader (CTL ImmunoSpot). Media containing an equivalent concentration of DMSO was used to measure background response levels, and 5 μg/ml of T. gondii ysates antigen (TLA) was used as a positive control.

ELISpot assays for production of IFN-γ by murine splenocytes were performed similarly, except that anti-mouse IFN-γ mAb (AN18) and biotinylated α-mouse IFN-γ mAb (R4-6A2) were used as cytokine-specific capture and detection antibodies instead. 5×10⁵ splenocytes were plated per well. All antibodies and reagents used for ELISpot assays were obtained from Mabtech (Cincinnati, Ohio). Cells were plated in at least 3 replicate wells for each condition. Results were expressed as number of spot forming cells (SFCs) per 10⁶ PBMCs or per 10⁶ murine splenocytes.

Immunizations and Challenge

Age-matched female HLA-A*0201 mice were inoculated subcutaneously (s.c.) at the base of the tail using a 30-gauge needle with pooled CD8⁺ T cell peptides as shown in Table 1, with pan DR epitope (PADRE), a universal helper T lymphocyte epitope emulsified in 3-deacylated monophosphoryl lipid A (GLA-SE). Controls were injected with PBS. Mice were boosted once at a 2-week interval. Mice were challenged intraperitoneally with 10,000 Pru-FLUC tachyzoites 10-14 days after the last immunization.

Ex Vivo Preparation of Murine Splenocytes

Three to five mice from each group were euthanized 7 to 14 days after the last immunization. Spleens were harvested, pressed through a 70 μm screen to form a single-cell suspension, and depleted of erythrocytes with ASK lysis buffer (160 mM NH₄Cl, 10 mM KHCO₃, 100 μM EDTA). Remaining splenocytes were washed twice with Hank's Balanced Salt Solution (HBSS) and resuspended in complete RPMI medium (RPMI-1640 supplemented with 2 mM L-GlutaMax [Invitrogen], 100 U/ml penicillin, 100 μg/ml streptomycin, 1 mM sodium pyruvate, 50 M β-mercaptoethanol, and 10% FCS) before use in subsequent in vitro assays.

In Vivo Bioluminescence Imaging

Mice infected with Pru-FLUC tachyzoites were imaged at day 7 post-challenge using the in vivo imaging system (IVIS; Xenogen, Alameda, Calif.) Mice were injected i.p. with 200 μl of D-luciferin and immediately anesthetized in an O₂-rich induction chamber with 2% isoflurane. After 12 min, mice were imaged in ventral positions and photonic emissions were assessed using Living image® 2.20.1 software (Xenogen). Data were presented as pseudocolor representations of light intensity and mean photons/s/region of interest (ROI).

Statistical Analyses

Statistical analyses for all in vitro assays were performed using a 2-tailed student's T test. Peptides were considered immunogenic in mice if they induced IFN-γ spot formation from immunized mice that was significant (P<0.05) relative to spot formation from control mice. Peptides and peptide pools were considered immunogenic in humans if they induced IFN-γ spot formation from PBMCs that was significant (P<0.05) relative to spot formation from the same cells incubated with media containing an equivalent concentration of DMSO. Each ELISpot experiment was replicated a minimum of twice. P values of ≦0.05 were considered significant.

Single letter designations are used for amino acids throughout.

II. Peptides and Lipopeptides

HLA-A03 supertype CD8⁺ T cell epitopes included: KSFKDILPK (SAG1₂₂₄₋₂₃₂) (SEQ ID NO: 4), AMLTAFFLR (GRA6₁₆₄₋₁₇₂) (SEQ ID NO: 5), and RSFKDLLKK (GRA7₁₃₄₋₁₄₂) (SEQ ID NO: 6). PADRE (AKFVAAWTLKAAA (SEQ ID NO: 7)) was the universal CD4 helper peptide used in vaccine constructs. Pam₂Cys (Pam₂-KSS) also was included. Peptides and lipopeptides were synthesized by Synthetic Biomolecules, San Diego at >90% purity. Additional HLA-A03 supertype bound peptides and their initial grouping into pools for in vitro studies are shown in Tables 2 and 3. A TLR4 agonist, a MLA mimetic, was synthesized by the Infectious Diseases Research Institute (Seattle, Wash.) as a stable oil-in-water emulsion. AMLTAFFLR (GRA6₁₆₄₋₁₇₂) (SEQ ID NO: 5) and additional new peptides were first dissolved in DMSO and then diluted in PBS.

Mice

HLA-A*1101/K^(b) transgenic mice were produced at Pharmexa-Epimmune (San Diego, Calif.) and bred at the University of Chicago. These HLA-A*1101/K^(b) transgenic mice express a chimeric gene consisting of the 1 and 2 domains of HLA-A*1101 and the 3 domain of H-2K^(b), and were created on a C57BL/6 background. All studies were conducted with approval of the Institutional Animal Care and Use Committee at the University of Chicago.

Parasites

Transgenic T. gondii used for in vivo challenges was derived from type II Prugniaud (Pru) strain and expresses the firefly luciferase (FLUC) gene constitutively by tachyzoites and bradyzoites. It was created, maintained and utilized as previously described in Saeij, et al. (2005) and Kim, S. K. et al. (2007).

Immunizations and Challenge

To evaluate peptide immunogenicity, HLA-A*1101 transgenic mice were inoculated subcutaneously (s.c.) at the base of the tail using a 30-gauge needle with single peptides or a mixture of CD8⁺ T cell peptides (50 μg of each peptide per mouse) and PADRE (AKFVAAWTLKAAA (SEQ ID NO: 7)) emulsified in 20 μg of MLA (TLR4 agonist) with or without Pam₂Cys. For immunization with lipopeptides, HLA-A*1101 mice received 20 nmol lipopeptide dissolved in PBS and emulsified in MLA. As controls, mice were injected with PBS. Mice were vaccinated twice at 3-week intervals. For challenge studies, mice were immunized with peptide emulsions and challenged intraperitoneally (i.p.) 14 days post-immunization using Type II parasites.

In Vivo Bioluminescence Imaging

Mice infected with 20,000 Pru-FLUC tachyzoites were imaged 7 days post-challenge using the in vivo imaging system (IVIS; Xenogen, Alameda, Calif.). Mice were injected i.p. with 200 μl of D-luciferin, anesthetized in an O₂-rich induction chamber with 2% isoflurane, and imaged after 12 minutes. Photonic emissions were assessed using Living image® 2.20.1 software (Xenogen). Data are presented as pseudocolor representations of light intensity and mean photons/s/region of interest (ROI).

ELISpot Assay

Murine splenocytes: Mice were euthanized 7 to 14 days after immunization. Spleens were harvested, pressed through a 70 μm screen to form a single-cell suspension, and depleted of erythrocytes with AKC lysis buffer (160 mM NH₄Cl, 10 mM KHCO₃, 100 μM EDTA). Splenocytes were washed twice with Hank's Balanced Salt Solution (HBSS) and resuspended in complete RPMI medium (RPMI-1640 supplemented with 2 mM L-GlutaMax [Invitrogen], 100 U/ml penicillin, 100 μg/ml streptomycin, 1 mM sodium pyruvate, 50 μM β-mercaptoethanol, and 10% FCS) before they were used in subsequent in vitro assays.

ELISpot assays with murine splenocytes were performed using α-mouse IFN-γ mAb (AN18) and biotinylated α-mouse IFN-γ mAb (R4-6A2) as the cytokine-specific capture antibodies. 5×10⁵ splenocytes were plated per well.

Human PBMC: PBMC were obtained, HLA haplotyped, processed and cryopreserved as described in Tan, T. G. (2010). ELISpot assays with human PBMCs were similar to those with murine splenocytes but used a-human IFN-γ mAb (1-D1K) with biotinylated a-human IFN-γ mAb (7B6-1) with 2×10⁵ PBMCs per well. All antibodies and reagents used for ELISpot assays were from Mabtech (Cincinnati, Ohio).

Both murine and human cells were plated in at least 3 replicate wells for each condition. Results were expressed as number of spot forming cells (SFCs) per 10⁶ PBMCs or per 10⁶ murine splenocytes.

Bioinformatic Predictions and MHC-Peptide Binding Assays

Protein sequences derived from GRA10, GRA15, SAG2C, SAG2D, SAG2X, SAG3, SRS9, BSR4, SPA, and MIC were analyzed for CD8⁺ T cell epitopes based on predicted binding affinity to HLA-A03 supertype molecules using ARB algorithms from immunoepitope database (IEDB) http://www.immuneepitope.org/. A total of 34 unique peptides IC₅₀<50 nM of all ranked nonameric peptides were selected. All protein sequences were from ToxoDB 5.1.

Quantitative assays to measure binding of peptides to HLA class I molecules are based on inhibition of binding of radiolabeled standard peptide. Assays were as described in Sidney, J., et al. Immunome Res 4, 2 (2008). Concentration of peptide yielding 50% inhibition of binding of radiolabeled probe peptide (IC₅₀) was calculated. Under conditions used, where [radiolabeled probe]<[MHC] and IC₅₀≧[MHC], measured IC₅₀ values are reasonable approximations of true K_(d) values.

Statistical Analyses

Statistical analyses for all in vitro assays were performed using 2-tailed student's T test. Two-tailed P values <0.05 were considered statistically significant. Peptides were considered immunogenic in mice if they induced IFN-γ spot formation from immunized mice that were significant (P<0.05) compared with spot formation from control mice. All mouse experiments were repeated at least twice, with 4-5 mice for each group.

III. Peptides and Adjuvants

HLA-B*0702-restricted peptides—GRA7₂₀₋₂₈ (LPQFATAAT (SEQ ID NO: 8)) and GRA3₂₇₋₃₅ (VPFVVFLVA (SEQ ID NO: 9)), PADRE (AKFVAAWTLKAAA (SEQ ID NO: 7)) and Pam₂Cys (Pam₂-KSS) (18) were synthesized by Synthetic Biomolecules, San Diego at >90% purity in lyophilized form. The TLR4 agonist was a MLA mimetic that was synthesized by the Infectious Diseases Research Institute (IDRI, Seattle, Wash.).

Mice

Female HLA-B*0702 transgenic mice express a chimeric HLA-B07/H2-D^(b) MHC Class I molecule, are on a C57BL/6 background and have been previously described (11), which were produced at Pharmexa-Epimmune (San Diego, Calif.) and bred at the University of Chicago. All studies were conducted with the approval of the Institutional Animal Care and Use Committee at the University of Chicago.

Analysis of Peptide Solubility

Peptides were dissolved in PBS followed by brief vortexing, to give a concentration of 5 mg/ml. Samples were centrifuged at 15,000 rpm at room temperature for 1 h. Supernatant concentrations were determined by measuring absorbance at 280 nm and Bradford assay. The percentage solubility of the samples was calculated.

Immunizations and Challenge

HLA-B*0702 mice were inoculated subcutaneously (s.c.) at the base of the tail using a 30-gauge needle with single peptides or a mixture of two of the identified B7 CD8⁺ T cell peptides, (amino acid sequence LPQFATAAT (SEQ ID NO: 8) [LT9] and amino acid sequence VPFVVFLVA (SEQ ID NO: 9) [VA9]) (50 μg of each peptide per mouse), with or without 50 μg PADRE and 50 μg Pam₂Cys emulsified in 20 μg of MLA (TLR4 agonist). Control mice were injected with PBS. Mice were boosted twice at 2-week intervals with a total of 50 μg of each peptide per mouse with each immunogen. For challenge studies, mice were challenged 14 days post immunization with peptide emulsions via intraperitoneal (i.p.) inoculation with Prugniaud—a type II strain luciferase expressing parasite.

ELISPOT Assay

Mice were euthanized 10 to 14 days after the last immunization. Spleens were harvested, pressed through a 70 μm screen to form a single-cell suspension, and depleted of erythrocytes with AKC lysis buffer (160 mM NH₄Cl, 10 mM KHCO₃, 100 μM EDTA). Murine ELISPOT assays were performed using anti-mouse IFN-γ mAb (AN18) and the biotinylated anti-mouse IFN-γ mAb (R4-6A2) and 5×10⁵ splenocytes were plated per well. All antibodies and reagents used for the ELISPOT assay were obtained from Mabtech (Cincinnati, Ohio). Cells were plated in at least 3 replicate wells for each condition. Results were expressed as the number of spot forming cells (SFCs) per 10⁶ murine splenocytes. Murine splenocytes were incubated with the relevant blocking antibody for 1.5 to 2 h at 37° C. and 5% CO₂ before they were seeded at 5×10⁵ cells per well. Anti-CD4⁺ antibody (RM4-5, BioLegend), anti-CD8 monoclonal antibody (53-6.7, BD Biosciences), and their relevant isotype control (Rat IgG_(2a), BD Biosciences) were added to each sample at a final concentration of 10 μg/ml. To assay for B7-restricted IFN-γ production, splenocytes were incubated with 0.5 μg of FcBlock™ (BD Biosciences) per 10⁶ cells for 10-15 min at 4° C. and washed before anti-HLA-B*0702 (BioLegend) mAb or its isotype control (mouse IgG_(2a), BioLegend) was added at a final concentration of 20 μg/ml.

T Cell Proliferation Assay

A splenocyte suspension containing 5×10⁶ cells/ml from immunized mice was plated into 96-well U-bottomed tissue culture plates (100 μl per well) along with 100 μl of each stimulant diluted to appropriate concentrations in complete RPMI1640. The stimulant used was peptide at 10 μg/ml. Concanavalin A at 10 μg/ml was used as a positive control and cells cultured with media alone were used as negative controls. The plates were incubated for 3 days in 5% CO2 at 37° C. and pulsed with 1 μCi [³H] thymidine per well for the final 18 h. The cells were then harvested onto a unifilter 96-well plate using a cell harvester (Packard Instrument, Meriden, Conn.). After drying, 25 μl of Microscint was added to each well and the filter plate was sealed and counted in a Top Count (Packard Instrument) to determine radioactivity incorporated into DNA. Results are expressed as the stimulation index (SI), calculated as the ratio between the mean counts per minute (cpm) for triplicate stimulated cultures and the mean counts per min for triplicate unstimulated cultures. SI values 2.0-fold greater than the SI of the control groups were considered to be significant.

In Vivo Bioluminescence Imaging

The transgenic T. gondii strain used for in vivo challenges was derived from the type II Prugniaud (Pru) strain and expresses the Firefly luciferase (FLUC) gene constitutively by tachyzoites and bradyzoites. Mice infected with Pru-FLUC tachyzoites were imaged at 5 days post-challenge using the in vivo imaging system (IVIS; Xenogen, Alameda, Calif.) as previously described. Mice were injected i.p. with 200 μl of D-luciferin (15.4 mg/ml) and immediately anesthetized in an O₂-rich induction chamber with 2% isoflurane. After 12 min, mice were imaged in ventral positions and photonic emissions were assessed using Living image® 2.20.1 software (Xenogen). Data were presented as pseudocolor representations of light intensity and mean photons/s/region of interest (ROI).

MHC-Peptide Binding Assays

Quantitative assays to measure the binding of peptides to HLA Class I molecules are based on the inhibition of binding of a radiolabeled standard peptide. Assays were performed as follows: 1 to 10 nM concentrations of radiolabeled peptides were coincubated with 1 M to 1 nM concentration of purified MHC in the presence of 1 to 3 uM human β₂-microglubulin. After 2 days, the binding of radiolabeled peptide to the corresponding MHC Class I molecule was determined by capturing MHC-peptide complexes on Greiner Lumitrac 600 microplates coated with the W6/32 antibody. The bound counts per minutes was measured using a Topcount microscintillation counter and the concentration of peptide yielding 50% inhibition of the binding of the radiolabeled probe peptide (IC₅₀) was calculated. Under the conditions used, where [radiolabeled probe]<[MHC] and IC₅₀≧[MHC], the measured IC₅₀ values are reasonable approximations of the true K_(d) values.

Statistical Analyses

There were 3-5 mice per group. PBMC were obtained from 3 seropositive and 4 seronegative donors. Each experiment was repeated at least twice. Statistical analyses for all in vitro assays were performed using a 2-tailed student's T-test. Two-tailed P values<0.05 were considered to be statistically significant. Peptides were considered immunogenic in mice if they induced IFN-γ spot formation or proliferation SI from immunized mice that was significant (P<0.05) compared with spot formation from control mice.

TABLE 1 Binding affinity of identified peptides and immunogenicity in human and transgenic mice Elicit  Elicit  SEQ Predicted Affinity IFN-γ (d) in IFN-γ (d) in Peptide ID IC50 nM (c) HLA- seropositive seronegative Immunogenicity Peptides (a) sequences NO: (b) A*0201 human human (e) in mice GRA6₂₄₋₃₂ VVFVVFMGV 1 76.3 14 + − − GRA6₂₉₋₃₇ FMGVLVNSL 2 26.6 18 + − + GRA3₂₅₋₃₃ FLVPFVVFL 3 8.6 <0.10 + − + SAG2C₃₈₋₄₆ FLSLSLLVI 11 34.1 736 + − + SAG2D₁₈₀₋₁₈₉ FMIAFISCFA 12 15.6 32 + − + SAG2X₄₄₋₅₂ FVIFACNFV 16 4.5 34 + − + SAG2X₃₅₁₋₃₅₉ FMIVSISLV 13 27.5 16 + − + SAG3₃₇₅₋₃₈₃ FLLGLLVHV 15 2.3 6.40 + − + SAG3₁₃₆₋₁₄₄ FLTDYIPGA 14 2.8 0.70 + − + SPA₁₂₋₂₀ ITMGSLFFV 17 10.7 0.16 + − + SPA₈₂₋₉₀ GLAAAVVAV 18 27.8 9.60 + − + MIC1₉₋₁₇ VLLPVLFGV 20 7.3 1.70 + − + MICA2/P₁₁₋₁₉ FAAAFFPAV 19 12.5 1.40 + − − (a) Peptides derived from proteins and the position within the proteins. (b) Peptides binding affinity to HLA-A02 were predicted using the ARB algorithms from immunoepitope database (IEDB). (c) Binding affinity was determined by MHC binding assay. (d) PBMC cells from four T. gondii-seropositive HLA-A02 humans and four seronegative ones were stimulated with peptides, the T cells that produce IFN-γ were tested by ELISPOT assay. (e) Splenic T cells were isolated from HLA-A*0201 mice 10-14 days after peptide immunization and tested for their ability to generate IFN-γ in response to peptide.

TABLE 2 Peptides utilized for screening CD8⁺ T cells (a) Predicted peptide candidates (b) MHC binding affinity for HLA-A03 supertype a HLA− PEPTIDE SEQ ID PREDICTED A*1101 ANTIGEN SEQUENCES NO: LENGTH LOCATION IC₅₀ nM POOL HLA-A*1101 GRA15 STSPFATRK 24 9 152-160 5 P1 HLA-A*1101 GRA15 ASTSPFATRK 25 10 150-159 18.2 HLA-A*1101 GRA10 AAAATPGLPK 26 10 568-577 9 HLA-A*1101 GRA10 AAATPGLPK 27 9 569-577 13.2 HLA-A*1101 GRA10 GVPAVPGLLK 28 10 507-516 17 HLA-A*1101 GRA10 SVVEENTMAK 29 10 865-874 25.1 HLA-A*1101 SAG2C STFWPCLLR 21 9 13-21 9.3 P2 HLA-A*1101 SAG2C ALLDHVFIEK 30 10 231-240 11.9 HLA-A*1101 SAG2C SSPQNIFYK 31 9 290-298 12.9 HLA-A*1101 SAG2C STTGVGETGK 32 10 163-172 28.4 HLA-A*1101 SAG2C GTEYSLALK 33 9 136-144 35.4 HLA-A*1101 SAG2D SSPQNIFYK 34 9 122-130 12.9 HLA-A*1101 SAG2D ALLEHVFIEK 35 10 1:63-72 20.2 P3 HLA-A*1101 SAG2D SSAQTFFYK 36 9 290-298 1.8 HLA-A*1101 SAG2D TVYFSCDPK 37 9 154-162 5.3 HLA-A*1101 SAG2D PSSAQTFFYK 38 10 289-298 17.9 HLA-A*1101 SAG3 VVGHVTLNK 39 9 80-88 15.4 HLA-A*1101 SAG3 KQYWYKIEK 40 9 145-153 19.3 HLA-A*1101 SRS9 TTCSVLVTVK 41 10 357-366 20.6 P4 HLA-A*1101 SRS9 AAASVQVPLK 42 10 140-149 29.9 HLA-A*1101 SRS9 AIQSQKWTLK 43 10 169-178 35 HLA-A*1101 BSR4 TTRFVEIFPK 44 10 284-293 10.3 HLA-A*1101 BSR4 VSGSLTLSK 45 9 83-91 21.1 HLA-A*1101 SPA SSAYVFSVK 22 9 250-258 9.3 P5 HLA-A*1101 SPA TSSAYVFSVK 46 10 249-258 12.2 HLA-A*1101 SPA YVFSVKELPK 47 10 253-262 18 HLA-A*1101 SPA KTEATYCYK 48 9 262-270 18.4 HLA-A*1101 SPA MTLMITRDSK 49 10 195-204 25.5 HLA-A*1101 SPA AVVSLLRLLK 23 10 89-98 6.5 HLA-A*1101 SPA VVSLLRLLK 50 9 90-98 7.2 HLA-A*1101 MIC1 LTLTFISTK 51 9 338-346 13.8 P6 HLA-A*1101 MIC3 SVQLGSFDK 52 9 32-40 12.9 HLA-A*1101 MIC4 SAVWFGVAK 53 9 16-24 17.2 HLA-A*1101 MICA2P GVMTPNQMVK 54 10 63-72 14.3 b SEQ HLA-A03-SUPERTYPE SUPERTYPE PEPTIDE ID POSI- HLA- HLA- HLA- HLA- HLA- HLA- ALLELES SEQUENCE NO: LENGTH PROTEIN TION A*0301 A*1101 A*3001 A*3101 A*3301 A*6801 BOUND STFWPCLLR 21 9 SAG2C 13-21 22 10 1272 1.2 3.4 0.97 5 SSAYVFSVK 22 9 SPA 250-258 12 10 1826 97 181 2.1 5 AVVSLLRLLK 23 10 SPA 89-98 17 34 8.1 1296 1100 94 4

TABLE 3 Peptides, their affinity for HLA-*1101, and their immunogenicity in humans and for transgenic mice. SEQ Affinity^(b) Elicit IFN-γ^(c) in Peptide ID HLA- Seropositive Seronegative Immunogenicity^(d) Sequences NO: Protein^(a) A*1101 human human in mice KSFKDILPK  4 SAG1₂₂₄₋₂₃₂ 54 + − + AMLTAFFLR  5 GRA6₁₆₄₋₁₇₂ 3.6 + − + RSFKDLLKK  6 GRA7₁₃₄₋₁₄₂ 14 + − − STFWPCLLR 21 SAG2C₁₃₋₂₁ 10 + − + SSAYVFSVK 22 SPA₂₅₀₋₂₅₈ 10 + − + AVVSLLRLLK 23 SPA₈₉₋₉₈ 34 + − + ^(a)Peptides derived from proteins and the position within the proteins ^(b)Binding affinity was performed by MHC binding assay. ^(c)PBMC from four T gondii-seropositive HLA-A03 supertype persons and four seronegative persons were stimulated with peptides, the T cell that produce IFN-γ were tested by ELISpot assay. ^(d)Splenic T cell were isolated from HLA-A*03 supertype(which includes the HLA-A*1101 haplotype) mice 10 to 14 days after peptide immunization and tested for their ability to generate IFN-γ in response to peptide

TABLE 4 Elicit IFN- Elicit IFN- Solu- γ (d) in γ (d) in Immuno- SEQ Predicted Affinitiy bility sero- sero- genicity Protec- Peptides Peptide ID IC50 nM (c) (d) in positive negative (e) in tive (a) sequences NO: (b) HLA*B0702 PBS (%) human human mice in mice GRA7₂₀₋₂₈ LPQFATAAT 8 62.4 14 99 + − + + GRA3₂₇₋₃₅ VPFVVFLVA 9 373.9 18 10 + − − − (a) Peptides derived from 2 proteins and the position within the protein. (b) Peptide-binding affinities to HLA-B*0702 were predicted using the ARB algorithms from the immunoepitope database (IEDB). IC50 is 50% inhibition of binding by a competitor. (c) Binding affinity was performed by MHC-binding assay. (d) Percentage solubility, values are determined by absorbance at 280 nm and Bradford assay. (e) PBMC cells from 4 T gondii-seropositive HLA-B07_humans and 3 seronegative ones were stimulated with GRA720-28 (LPQFATAAT (SEQ ID NO: 8)) and GRA327-35 (VPFVVFLVA (SEQ ID NO: 9)); the T cells that produce IFN-γ were tested by ELISPOT assay. (f) Splenic T cells were isolated from HLA-A*0702 mice 2 weeks after peptide immunization and tested for their ability to generate IFN-γ in response to peptide. (−), Not immunogenic at any dose. (g) Protective HLA-B*0702 in transgenic mice.

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1. A plurality of peptides selected from the group consisting of FLSLSLLVI (SEQ ID NO: 11), FMIAFISCFA (SEQ ID NO: 12), FVIFACNFV (SEQ ID NO: 16), FMIVSISLV (SEQ ID NO: 13), FLLGLLVHV (SEQ ID NO: 15), FLTDYIPGA (SEQ ID NO: 14), ITMGSLFFV (SEQ ID NO: 17), GLAAAVVAV (SEQ ID NO: 18), VLLPVLFGV (SEQ ID NO: 20), FAAAFFPAV (SEQ ID NO: 19), VVFVVFMGV (SEQ ID NO: 1), FMGVLVNSL (SEQ ID NO: 2), FLVPFVVFL (SEQ ID NO: 3) and combinations thereof.
 2. The peptides of claim 1 further defined as displaying high affinity binding to HLA-AO2 proteins.
 3. An immunological composition comprising a plurality of peptides of claim
 1. 4. The composition of claim 3 further comprising PADRE and adjuvants.
 5. An immunosense epitope vaccine that confers protection against parasite infection.
 6. The vaccine of claim 5 wherein the parasite is Toxoplasma gondii.
 7. The vaccine of claim 5 comprising a plurality of peptides of claim 1 in an immunological composition.
 8. A plurality of peptides that elicit production of IFN-γ from PBMC of HLA-A03 supertype subjects seropositive for T. gondii infection when in an immunologic composition, but do not elicit production of IFN-γ from seronegative controls, the peptides selected from the group consisting of: KSFKDILPK (SEQ ID NO: 4), AMLTAFFLR (SEQ ID NO: 5) and RSFKDLLKK (SEQ ID NO: 6) and combinations thereof.
 9. The peptides of claim 8 further defined as displaying high affinity binding to HLA-AO3 proteins.
 10. An immunological composition comprising the plurality of peptides of claim 8, PADRE (AKFVAAWTLKAAA (SEQ ID NO: 7)) and an out-in water emulsion that includes a synthetic MLS deriviation.
 11. T. gondii specific epitopes consisting of LPQFATAAT (SEQ ID NO: 8) and VPFVVFLVA (SEQ ID NO: 9).
 12. A vaccine comprising a peptide selected from the group consisting of SAG2C₃₈₋₄₆, SAG2D₁₈₀₋₁₈₉, SAG2X₄₄₋₅₂, SAG2X₃₅₁₋₃₅₉, SAG3₁₃₆₋₁₄₄, SAG³ ₃₇₅₋₃₈₃, SPA₁₂₋₂₀, SPA₈₂₋₉₀, MIC1₉₋₁₇, MICA2P₁₁₋₁₉, GRA⁶ ₂₄₋₃₂, GRA6₂₉₋₃₇, and GRA3₂₅₋₃₃.
 13. A vaccine comprising a peptide selected from the group consisting of: SAG1₂₂₄₋₂₃₂; GRA6₁₆₄₋₁₇₂; and GRA7₁₃₄₋₁₄₂.
 14. The vaccine of claim 12, further comprising an adjuvant.
 15. The vaccine of claim 12, further comprising PADRE.
 16. A vaccine comprising at least one peptide selected from the group consisting of FLSLSLLVI (SEQ ID NO: 11), FMIAFISCFA (SEQ ID NO: 12), FVIFACNFV (SEQ ID NO: 16), FMIVSISLV (SEQ ID NO: 13), FLLGLLVHV (SEQ ID NO: 15), FLTDYIPGA (SEQ ID NO: 14), ITMGSLFFV (SEQ ID NO: 17), GLAAAVVAV (SEQ ID NO: 18), VLLPVLFGV (SEQ ID NO: 20), FAAAFFPAV (SEQ ID NO: 19), VVFVVFMGV (SEQ ID NO: 1), FMGVLVNSL (SEQ ID NO: 2), FLVPFVVFL (SEQ ID NO: 3), KSFKDILPK (SEQ ID NO: 4), AMLTAFFLR (SEQ ID NO: 5), RSFKDLLKK (SEQ ID NO: 6), SAG2C₃₈₋₄₆, SAG2D1₁₈₀₋₁₈₉, SAG2X₄₄₋₅₂, SAG2X₃₅₁₋₃₅₉, SAG3₁₃₆₋₁₄₄, SAG3₃₇₅₋₃₈₃, SPA₁₂₋₂₀, SPA₈₂₋₉₀, MIC1₉₋₁₇, MICA2P₁₁₋₁₉, GRA⁶ ₂₄₋₃₂, GRA6₂₉₋₃₇, GRA3₂₅₋₃₃, SAG1₂₂₄₋₂₃₂; GRA⁶ ₁₆₄₋₁₇₂; and GRA7₁₃₄₋₁₄₂.
 17. The vaccine of claim 16, comprising at least two of the peptides selected from the group consisting of FLSLSLLVI (SEQ ID NO: 11), FMIAFISCFA (SEQ ID NO: 12), FVIFACNFV (SEQ ID NO: 16), FMIVSISLV (SEQ ID NO: 13), FLLGLLVHV (SEQ ID NO: 15), FLTDYIPGA (SEQ ID NO: 14), ITMGSLFFV (SEQ ID NO: 17), GLAAAVVAV (SEQ ID NO: 18), VLLPVLFGV (SEQ ID NO: 20), FAAAFFPAV (SEQ ID NO: 19), VVFVVFMGV (SEQ ID NO: 1), FMGVLVNSL (SEQ ID NO: 2), FLVPFVVFL (SEQ ID NO: 3), KSFKDILPK (SEQ ID NO: 4), AMLTAFFLR (SEQ ID NO: 5), RSFKDLLKK (SEQ ID NO: 6), SAG2C₃₈₋₄₆, SAG2D₁₈₀₋₁₈₉, SAG2X₄₄₋₅₂, SAG2X₃₅₁₋₃₅₉, SAG3₁₃₆₋₁₄₄, SAG³ ₃₇₅₋₃₈₃, SPA₁₂₋₂₀, SPA₈₂₋₉₀, MIC1₉₋₁₇, MICA2P₁₁₋₁₉, GRA⁶ ₂₄₋₃₂, GRA⁶ ₂₉₋₃₇, GRA³ ₂₅₋₃₃, SAG1₂₂₄₋₂₃₂; GRA⁶ ₁₆₄₋₁₇₂; and GRA7₁₃₄₋₁₄₂.
 18. The vaccine of claim 17, comprising at least three of the peptides selected from the group consisting of FLSLSLLVI (SEQ ID NO: 11), FMIAFISCFA (SEQ ID NO: 12), FVIFACNFV (SEQ ID NO: 16), FMIVSISLV (SEQ ID NO: 13), FLLGLLVHV (SEQ ID NO: 15), FLTDYIPGA (SEQ ID NO: 14), ITMGSLFFV (SEQ ID NO: 17), GLAAAVVAV (SEQ ID NO: 18), VLLPVLFGV (SEQ ID NO: 20), FAAAFFPAV (SEQ ID NO: 19), VVFVVFMGV (SEQ ID NO: 1), FMGVLVNSL (SEQ ID NO: 2), FLVPFVVFL (SEQ ID NO: 3), KSFKDILPK (SEQ ID NO: 4), AMLTAFFLR (SEQ ID NO: 5), RSFKDLLKK (SEQ ID NO: 6), SAG2C₃₈₋₄₆, SAG2D₁₈₀₋₁₈₉, SAG2X₄₄₋₅₂, SAG2X₃₅₁₋₃₅₉, SAG3₁₃₆₋₁₄₄, SAG3₃₇₅₋₃₈₃, SPA₁₂₋₂₀, SPA₈₂₋₉₀, MIC1₉₋₁₇, MICA2P₁₁₋₁₉, GRA⁶ ₂₄₋₃₂, GRA⁶ ₂₉₋₃₇, GRA³ ₂₅₋₃₃, SAG1₂₂₄₋₂₃₂; GRA6₁₆₄₋₁₇₂; and GRA7₁₃₄₋₁₄₂.
 19. A vaccine comprising at least one peptide that is at least 88% homologous to a peptide selected from the group consisting of FLSLSLLVI (SEQ ID NO: 11), FMIAFISCFA (SEQ ID NO: 12), FVIFACNFV (SEQ ID NO: 16), FMIVSISLV (SEQ ID NO: 13), FLLGLLVHV (SEQ ID NO: 15), FLTDYIPGA (SEQ ID NO: 14), ITMGSLFFV (SEQ ID NO: 17), GLAAAVVAV (SEQ ID NO: 18), VLLPVLFGV (SEQ ID NO: 20), FAAAFFPAV (SEQ ID NO: 19), VVFVVFMGV (SEQ ID NO: 1), FMGVLVNSL (SEQ ID NO: 2), FLVPFVVFL (SEQ ID NO: 3), KSFKDILPK (SEQ ID NO: 4), AMLTAFFLR (SEQ ID NO: 5), RSFKDLLKK (SEQ ID NO: 6), SAG2C₃₈₋₄₆, SAG2D₁₈₀₋₁₈₉, SAG2X₄₄₋₅₂, SAG2X₃₅₁₋₃₅₉, SAG3₁₃₆₋₁₄₄, SAG3₃₇₅₋₃₈₃, SPA₁₂₋₂₀, SPA₈₂₋₉₀, MIC1₉₋₁₇, MICA2P₁₁₋₁₉, GRA6₂₄₋₃₂, GRA6₂₉₋₃₇, GRA³ 25-33, SAG1₂₂₄₋₂₃₂; GRA6₁₆₄₋₁₇₂; and GRA7₁₃₄₋₁₄₂.
 20. The plurality of peptides of claim 1 further defined as eliciting production of IFN-γ from PBMC of HLA-A02 supertype subjects seropositive for T. Gondii infection when in an immunologic composition, but not elicitng production of IFN-γ from seronegative controls. 